Medi-Source, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Medi-Source, Inc. has 4 FDA 510(k) cleared medical devices. Based in Syosset, US.
Historical record: 4 cleared submissions from 1989 to 1990. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Medi-Source, Inc. Filter by specialty or product code using the sidebar.
4 devices
Cleared
Aug 22, 1990
GEOHESIVE (TM), MODEL NUMBERS 1022L, 1023L, 1026L
Neurology
22d
Cleared
Mar 29, 1989
GELLHORN PESSARY 33410 VARIOUS SIZES
Obstetrics & Gynecology
51d
Cleared
Mar 15, 1989
BERMAN TYPE AIRWAY #59422-59429 VARIOUS SIZES
Anesthesiology
37d
Cleared
Feb 17, 1989
BITE BLOCK #59430
Neurology
11d