American Bio Medica Corp.
FDA 510(k) & PMA Approved Devices — 30 products
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Total Devices30
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K170222 | Rapid Tox Cup II | LAF | 2017-08-15 | View |
| 510(k) | K073078 | RAPID TOX CUP | LAG | 2008-05-30 | View |
| 510(k) | K060760 | RAPIDONE-BUPRENORPHINE TEST | DJG | 2006-08-07 | View |
| 510(k) | K053422 | RAPIDONE-COCAINE-150 TEST | DIO | 2006-06-15 | View |
| 510(k) | K053359 | RAPIDTOX | DKZ | 2006-05-25 | View |
| 510(k) | K041696 | RAPID READER | DKZ | 2005-07-12 | View |
| 510(k) | K041712 | 'RAPIDTEC 4' TEST | DIS | 2004-11-03 | View |
| 510(k) | K030835 | 'RAPID ONE' - PROPOXYPHENE TEST | JXN | 2003-05-22 | View |
| 510(k) | K023869 | 'RAPIDTEC'-5M-MULTIPLE DIP TEST | DJR | 2003-04-30 | View |
| 510(k) | K021114 | 'RAPIDTEC' 5A MULTIPLE DIP TEST | DKZ | 2002-07-23 | View |
| 510(k) | K014101 | RAPIDONE-OXY TEST | DJG | 2002-03-20 | View |
| 510(k) | K013180 | RAPIDONE-ECSTASY TEST | DJC | 2001-11-26 | View |
| 510(k) | K012164 | 'RAPIDONE'-METHADONE TEST | DJR | 2001-11-20 | View |
| 510(k) | K012159 | RAPID DRUG SCREEN | DKZ | 2001-07-25 | View |
| 510(k) | K002447 | MODIFICATION TO RAPID DRUG SCREEN 9-PANEL | DKZ | 2000-11-16 | View |
| 510(k) | K992720 | RAPIDONE- BENZODIAZEPINE TEST | JXM | 2000-04-03 | View |
| 510(k) | K992451 | RAPIDONE- BARBITURATE TEST | DIS | 2000-04-03 | View |
| 510(k) | K993961 | RAPID DRUG SCREEN 3-PANEL TEST FOR COCAINE, MARIJUANA (THC) (CANNABINOIDS) AND OPIATES (3 PANEL TEST FOR CTO) | LDJ | 2000-01-24 | View |
| 510(k) | K993151 | RADID DRUG SCREEN 5-PANEL TEST | DJG | 2000-01-10 | View |
| 510(k) | K993796 | RAPID DRUG SCREEN 5-PANEL DRUG SCREENING TEST FOR COCAINE, MARIJUANA, OPIATES, AMPHETAMINE AND METHAMPHETAMINE | LDJ | 1999-12-21 | View |
No matching devices.
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