Pace Tech, Inc.
FDA 510(k) medical device clearances.
Top product codes for Pace Tech, Inc.
Recent clearances by Pace Tech, Inc.
- K951226 — VITALMAX 4000/MINIPACK 3100/3000
- K953795 — VITALMAX 4100
- K944541 — HANDYPACK 911SC
- K945385 — VITALMAX 800 PLUS/VITALMAX 810 PLUS/MINIPACK 300
- K925701 — MINIPACK 911-STC
- K934385 — MINIPACK 3100/3000 MODIFICATION
- K933624 — VITALMAX 4000
- K930559 — VITALMAX 800-C
- K912835 — MINI-PACK 911 SERIES
- K912880 — VITALMAX 510/520
- K913263 — VITALMAX 830 SERIES
- K905274 — VITALMAX 2100/2200
- K901066 — VITALMAX 500 PULSE OXIMETER W/TEMP. AND RESPIRA.
- K900451 — VITALMAX 800 NON-INVASIVE VITAL SIGN MONITOR/PULSE
- K901612 — VITALMAX 2000 ECG MONITOR W/NON-INVASIVE BLOOD-PRE
- K900866 — OXIMAX 700
- K900843 — OXIMAX 100
- K880351 — VITAL SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.