Medical Device Manufacturer · US , Washington , DC

American Bio Medica Corp. - FDA 510(k) Cleared Devices

30 submissions · 30 cleared · Since 1997

Total

Cleared

Denied

American Bio Medica Corp. has 30 FDA 510(k) cleared toxicology devices. Based in Washington, US.

Historical record: 30 cleared submissions from 1997 to 2017.

Browse the complete list of FDA 510(k) cleared toxicology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by American Bio Medica Corp.

30 devices

1-12 of 30

RAPIDONE-BUPRENORPHINE TEST

K060760 · DJG

Toxicology · 139d

Cleared Jun 15, 2006

RAPIDONE-COCAINE-150 TEST

'RAPID ONE' - PROPOXYPHENE TEST

K030835 · JXN

Toxicology · 66d

Cleared Apr 30, 2003

'RAPIDTEC'-5M-MULTIPLE DIP TEST

K023869 · DJR

Toxicology · 161d

Cleared Jul 23, 2002

'RAPIDTEC' 5A MULTIPLE DIP TEST

RAPIDONE-ECSTASY TEST

K013180 · DJC

Toxicology · 63d

American Bio Medica Corp. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by American Bio Medica Corp.

Filters