Sims Portex, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Sims Portex, Inc. has 12 FDA 510(k) cleared medical devices. Based in Keene, US.
Historical record: 12 cleared submissions from 1998 to 2001. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Sims Portex, Inc. Filter by specialty or product code using the sidebar.
12 devices
Cleared
Jul 12, 2001
HYPODERMIC NEEDLE-PRO NEEDLE WITH NEEDLE PROTECTION DEVICE
General Hospital
22d
Cleared
Feb 05, 2001
ELECTROSTATIC HYDROPHOBIC BREATHING FILTER
General Hospital
200d
Cleared
Dec 14, 2000
BREATHING FILTER FOR DISPOSABLE ANESTHESIA BREATHING CIRCUIT
General Hospital
121d
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
Feb 22, 2000
SIMS PORTEX ANESTHESIA CATHETER
General Hospital
64d
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
Apr 21, 1998
PRO-VENT, PULSATOR ARTERIAL BLOOD SAMPLING SYRINGES
Chemistry
33d
Cleared
Feb 24, 1998
PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KIT WITH SPECIALTY TRACHEOSTOMY...
Anesthesiology
18d