Cardiac Pacemakers, Inc.
FDA 510(k) medical device clearances.
Top product codes for Cardiac Pacemakers, Inc.
Recent clearances by Cardiac Pacemakers, Inc.
- K093969 — ACUITY BREAK-AWAY GUIDE CATHETER
- K080154 — ACUITY UNIVERSAL CUTTER
- K934727 — REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER
- K920601 — ASTRA T2, ASTRA T4, ASTRA T6
- K912379 — PDT CARRYALL TRANSMITTER, VARIOUS MODELS
- K905674 — LEAD STYLET
- K900498 — MODIFIED BETATRON IV INSULIN INFUSION SYSTEM
- K894738 — MODEL 6888 LEAD TUNNELER
- K890785 — ASTRA T2, T3, T4, T6 PULSE GENERATORS NEW PACKAGE
- K875147 — TORQUE HEX WRENCH
- K872774 — BETATRON IV SYSTEM
- K865013 — ASTRA T2, T4 AND T6
- K863046 — ULTRA SOFTWARE MODULE: MODEL 2016
- K863045 — PROGRAMMER MODEL 2035/ELECTROGRAM CABLE MODEL 6580
- K863000 — ASTRA 2,3,4 AND 6: CHIP REVISION
- K860585 — ASTRA T2, T3, T4 & T6 MULTIPROGRAM PULSE GENERATOR
- K860584 — SOFTWARE MODULE/2035 PROG AND ASTRA/T PULSE GEN
- K855171 — TELEMETRY WAND MODEL
- K852060 — INFUSION SETS MODELS 9120,9121,9125, 9122 & 9123
- K842394 — ASTRA 2, ASTRA 3, 4 & 6
- K842364 — HANDHELD PACEMAKER PROGRAMMER & SOFTWAR
- K843060 — SENTRA
- K833306 — BETATRON I AMBULATORY INSULIN PUMP
- K831216 — COMMAND ULTRA II
- K831161 — COMMAND ULTRA I
- K831160 — LEAD ADAPTERS #'S 6016,6022,6017 ETC
- K831259 — RESERVOIR 1.5CC #9210 W/25 GAUGE/NEEDLE
- K830382 — COMMAND ULTRA II
- K822857 — CPI PRINTER
- K823204 — BETATRON II
- K822774 — 9110 SYRINGE
- K822775 — INFUS. SETS-9120-50 CM & 9121-100 CM,EXT
- K822776 — TEFLON CANNULA
- K822309 — COMMAND NP
- K820230 — PACEMAKER PROGRAMMER 2030
- K820231 — COMMAND ULTRA I
- K820073 — OPEN LOOP AMBULATORY INSULIN INFUSION
- K813534 — COMMAND P5
- K812917 — PORTABLE LIDOCAINE INFUSION PUMP
- K811401 — COMMAND P5(UNIPOLAR PULSE GENERATOR)
- K811402 — COMMAND P5(BIPOLAR PULSE GENERATOR)
- K811217 — PACEMAKER PROGRAMMER #2010
- K811774 — OPEN LOOP AMBULATORY INFUSION DEVICE
- K802352 — MICRO THIN-DII, #0521
- K802353 — MICRO THIN-PII, #0523
- K803034 — MICROTHIN-PII BIPOLAR PULSE GEN. #0623
- K803035 — MICROTHIN-PII BIPOLAR PULSE GEN. #0621
- K802058 — MAPPING PROBE MODEL #6540
- K802409 — MICROTHIN-DI BIPOLAR PULSE GENERATOR
- K802410 — MICROTHIN-PI BIPOLAR PULSE GENERATOR
- K802077 — UNIPOLAR TO BIPOLAR PULSE GEN. ADAPTER
- K802076 — STIFF STYLETS
- K802089 — CARDIOTRAK
- K801121 — MICROTHIN-P1 (MOD. 0622)
- K801122 — MICROTHIN-D1 (MOD. 0620)
- K800026 — MICROTHIN-DI
- K800027 — MICROTHIN-PI
- K792580 — PACEMAKER PROGRAMMER
- K790503 — CARDIOTEST 2200
- K790432 — MICROLITH MODELS 505;605;507;607;703;803
- K790276 — MINILITH AND MICROLITH
- K782022 — MICROLITH A MODEL 703
- K782023 — MICROLITH A MODEL 803
- K772238 — PULSE GENERATOR, UNIPOLAR, PROGRAMABLE
- K772239 — PULSE GENERATOR, BIPOLAR, PROGRAMMABLE
- K772240 — PULSE GENERATOR, UNIPOLAR, DEMAND
- K772241 — PULSE GENERATOR, BIPOLAR, DEMAND
- K770880 — GENERATOR, PULSE, UNIPOLAR, #508
- K770881 — GENERATOR, PULSE, BIPOLAR 3608
- K770716 — GENERATOR, PULSE, UNIPOLAR, MODEL #504
- K770715 — GENERATOR, PULSE, BIPOLAR, MODEL #604
- K770243 — ELGILOY STYLET
- K770197 — UNIPOLAR, ASYNCHRONOUS PULSE GENERATOR
- K770198 — BIPOLAR ASYNCHRONOUS PULSE GENERATOR
- K770199 — LEAD EXTENDER MODEL 6516
- K770042 — ADAPTER, LEAD, GENERAL ELECTRIC
Data sourced from openFDA. This site is unofficial and independent of the FDA.