Martell Medical Products, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Martell Medical Products, Inc. has 7 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 7 cleared submissions from 1981 to 1995. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Martell Medical Products, Inc. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Apr 14, 1995
LEUR TIP CAP, VLT CAP(TM)
Chemistry
158d
Cleared
Dec 05, 1994
PISTON SYRINGE
Anesthesiology
59d
Cleared
Jul 06, 1984
MARK5 ARTERIAL BLOOD GAS KIT
General Hospital
66d
Cleared
Oct 21, 1982
MDM ARTERIAL BLOOD GAS KIT
Anesthesiology
36d
Cleared
Sep 28, 1982
ARTERIAL LINE KIT
General Hospital
14d
Cleared
May 14, 1982
A-LINER
General Hospital
24d
Cleared
Oct 09, 1981
MDM ARTERIAL BLOOD GAS SYRINGE
General Hospital
31d