Martech Medical Products, Inc. is one of 25971 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Martech Medical Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MARTECH ENDOSCOPIC INJECTION NEEDLE, MARKSMAN ARTERIAL BLOOD GAS SYRINGE, PRO2 OXYGEN ANALYZER
7
Total
6
Cleared
0
Denied
Martech Medical Products, Inc. has 6 FDA 510(k) cleared medical devices. Based in Riverside, US.
Historical record: 6 cleared submissions from 1989 to 1996.
Browse the FDA 510(k) cleared devices submitted by Martech Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Martech Medical Products, Inc.
7 devices
Cleared
May 01, 1996
MARTECH ENDOSCOPIC INJECTION NEEDLE
Gastroenterology & Urology
86d
Cleared
Aug 03, 1993
MARKSMAN ARTERIAL BLOOD GAS SYRINGE
Chemistry
109d
Cleared
Mar 05, 1993
PRO2 OXYGEN ANALYZER
Anesthesiology
287d
Cleared
Feb 23, 1993
ACCESSORY TO PISTON SYRINGE
General Hospital
88d
Cleared
Sep 16, 1992
NEOLINE(TM)
Anesthesiology
329d
Cleared
Oct 15, 1991
MARKSMAN ARTERIAL BLOOD GAS SYRINGE
Chemistry
222d
Cleared
Apr 03, 1989
NEEDLE GUARD(TM)
General Hospital
62d