Sims Portex, Inc.
Sims Portex, Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2001.
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.