Anarobe Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Anarobe Systems - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Anarobe Systems has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1984 to 1984. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Anarobe Systems Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Anarobe Systems
7 devices
Cleared
Aug 17, 1984
TRIPLE SUGAR IRON
Microbiology
28d
Cleared
Aug 17, 1984
MUELLER HINTON BROTH
Microbiology
28d
Cleared
Aug 07, 1984
ORNITHINE INDOLE MOTILITY
Microbiology
18d
Cleared
Aug 03, 1984
TRYPTICASE SOY BROTH
Chemistry
14d
Cleared
Aug 03, 1984
BRAIN HEART INFUSION BROTH
Microbiology
14d
Cleared
Aug 03, 1984
LYSINE IRON AGAR
Microbiology
14d
Cleared
Aug 03, 1984
CHRISTENSEN'S UREA AGAR
Microbiology
14d