The following data is part of a premarket notification filed by American Bio Medica Corp. with the FDA for Modification To Rapid Drug Screen 9-panel.
| Device ID | K002447 |
| 510k Number | K002447 |
| Device Name: | MODIFICATION TO RAPID DRUG SCREEN 9-PANEL |
| Classification | Enzyme Immunoassay, Amphetamine |
| Applicant | AMERICAN BIO MEDICA CORP. 1001 G STREET, NW SUITE 500W Washington, DC 20001 |
| Contact | John B Dubeck |
| Correspondent | John B Dubeck AMERICAN BIO MEDICA CORP. 1001 G STREET, NW SUITE 500W Washington, DC 20001 |
| Product Code | DKZ |
| Subsequent Product Code | DIO |
| Subsequent Product Code | DIS |
| Subsequent Product Code | DJC |
| Subsequent Product Code | DJG |
| Subsequent Product Code | JXM |
| Subsequent Product Code | LCM |
| Subsequent Product Code | LDJ |
| Subsequent Product Code | LFI |
| CFR Regulation Number | 862.3100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-08-09 |
| Decision Date | 2000-11-16 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10694644350781 | K002447 | 000 |
| 10694644350798 | K002447 | 000 |