Neotech Products, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Neotech Products, Inc. has 6 FDA 510(k) cleared medical devices. Based in Chatsworth, US.
Historical record: 6 cleared submissions from 1988 to 2002. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Neotech Products, Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Jan 03, 2002
NEOLEAD
Cardiovascular
227d
Cleared
Jul 23, 1993
URINARY DRAINAGE BAG CADDY
Gastroenterology & Urology
142d
Cleared
Sep 02, 1992
URO-TOTE LEG BAG
Gastroenterology & Urology
183d
Cleared
Apr 19, 1989
NEOTECH MUCUS TRAP W/CATHETER
Anesthesiology
83d
Cleared
Jun 17, 1988
NEOTECH UNIVERSAL ADAPTER
Anesthesiology
23d
Cleared
May 06, 1988
NEOTECH MECONIUM ASPIRATOR (STERILE)
Anesthesiology
92d