Biolog, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biolog, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Biolog, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1981 to 1985. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Biolog, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biolog, Inc.
6 devices
Cleared
May 23, 1985
DISPOSABLE UROSTOMY POUCH
Gastroenterology & Urology
87d
Cleared
May 23, 1985
DISPOS. DRAINABEL POUCH FOR ILEOSTOMY/COLOSTOMY
Gastroenterology & Urology
87d
Cleared
Jun 12, 1981
GC CULTURE MEDIUM
Microbiology
35d
Cleared
Jun 12, 1981
SELECTIVE GC CULTURE MEDIUM
Microbiology
35d
Cleared
Jun 12, 1981
JEMBEC TRANSPORT SYSTEM
Microbiology
35d
Cleared
Jun 12, 1981
GC TTANSPORT SYSTEM
Microbiology
35d