Sims Portex, Inc.
FDA 510(k) medical device clearances.
Top product codes for Sims Portex, Inc.
Recent clearances by Sims Portex, Inc.
- K011925 — HYPODERMIC NEEDLE-PRO NEEDLE WITH NEEDLE PROTECTION DEVICE; HYPODERMIC NEEDLE-PRO SYRINGE & NEEDLE WITH NEEDLE PROTECTIO
- K002201 — ELECTROSTATIC HYDROPHOBIC BREATHING FILTER
- K002506 — BREATHING FILTER FOR DISPOSABLE ANESTHESIA BREATHING CIRCUIT
- K001318 — CPAP SYSTEM, MODEL 102001
- K993619 — CSECURE COMBINED SPINAL/EPIDURAL ANESTHESIA SYSTEM WITH LOCK
- K994275 — SIMS PORTEX ANESTHESIA CATHETER
- K991861 — 1ST RESPONSE INFANT MANUAL RESUSCITATOR, BAG RESEVOIR, 1ST RESPONSE PEDIATRIC MANUAL RESUSCITATOR, BAG RESERVOIR, 1ST RE
- K992471 — SIMS PORTEX EPIDURAL CATHETER, 20G MODEL# 4910-16/17; 21G MODEL# 4910-18
- K992057 — IST RESPONSE MANUAL RESUSCITATOR, MODELS, 008000, 008003,008006
- K983858 — SPINAL ANESTHESIA NEEDLES AND INTRODUCER NEEDLES
- K981035 — PRO-VENT, PULSATOR ARTERIAL BLOOD SAMPLING SYRINGES
- K980466 — PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KIT WITH SPECIALTY TRACHEOSTOMY TUBE AND DISPOSABLE INNER CANNULA
Data sourced from openFDA. This site is unofficial and independent of the FDA.