Medical Device Manufacturer · US , Keene , NH

Sims Portex, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1998

12

Total

12

Cleared

0

Denied

FDA 510(k) Regulatory Record - Sims Portex, Inc. Anesthesiology ✕

7 devices

1-7 of 7

Cleared Jul 20, 2000

CPAP SYSTEM, MODEL 102001

Anesthesiology · 85d

Cleared Apr 28, 2000

CSECURE COMBINED SPINAL/EPIDURAL ANESTHESIA SYSTEM WITH LOCK

Anesthesiology · 185d

Cleared Jan 18, 2000

1ST RESPONSE INFANT MANUAL RESUSCITATOR, BAG RESEVOIR, 1ST RESPONSE PEDIATRIC...

Anesthesiology · 231d

Cleared Oct 22, 1999

SIMS PORTEX EPIDURAL CATHETER, 20G MODEL# 4910-16/17

Anesthesiology · 88d

Cleared Sep 13, 1999

IST RESPONSE MANUAL RESUSCITATOR, MODELS, 008000, 008003,008006

Anesthesiology · 87d

Cleared Jan 29, 1999

SPINAL ANESTHESIA NEEDLES AND INTRODUCER NEEDLES

Anesthesiology · 88d

Cleared Feb 24, 1998

PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KIT WITH SPECIALTY TRACHEOSTOMY...

Anesthesiology · 18d