# American Bio Medica Corp.

- Location (FDA's records): Washington, DC
- FDA decisions: 30 (1997–2017): 30 510(k) clearances
- Product codes: DKZ (9), DIO (4), DJG (4), LDJ (3), DJR (2), DIS (2), DOD (1), JXN (1), LAF (1), LAG (1), DJC (1), JXM (1)
- Predicates its devices cite: 17 (14 its own); citations of its devices by later devices: 22 (14 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Biosite Incorporated: 2 (https://510kreport.com/company/biosite)
- Medtox Diagnostics, Inc.: 1 (https://510kreport.com/company/medtox-diagnostics)

## Firms that cite its devices most
- Starplex Scientific, Inc.: 4 (https://510kreport.com/company/starplex-scientific)
- Psychemedics Corp.: 1 (https://510kreport.com/company/psychemedics)
- W.H.P.M., Inc.: 1 (https://510kreport.com/company/whpm)
- Omega Laboratories, Inc.: 1 (https://510kreport.com/company/omega-laboratories)
- Microgenics Corp.: 1 (https://510kreport.com/company/microgenics)

## Its most-cited devices
- K012159: Rapid Drug Screen (2001), cited by 3
- K002447: Modification to Rapid Drug Screen 9-Panel (2000), cited by 3
- K014101: Rapidone-Oxy Test (2002), cited by 3
- K990822: Rapidone - Cocaine Test (1999), cited by 2
- K984525: Rapid Drug Screen 5-Panel with Methamphetamine Test (1999), cited by 2
- K041712: 'Rapidtec 4' Test (2004), cited by 2

## Recent decisions
- K170222: Rapid Tox Cup II (Aug 15, 2017)
- K073078: Rapid Tox Cup (May 30, 2008)
- K060760: Rapidone-Buprenorphine Test (Aug 7, 2006)
- K053422: Rapidone-Cocaine-150 Test (Jun 15, 2006)
- K053359: Rapidtox (May 25, 2006)
- K041696: Rapid Reader (Jul 12, 2005)
- K041712: 'Rapidtec 4' Test (Nov 3, 2004)
- K030835: 'Rapid One' - Propoxyphene Test (May 22, 2003)

Source page: https://510kreport.com/company/american-bio-medica