The following data is part of a premarket notification filed by Microgenics Corp. with the FDA for Cedia Dau Benzodiazepine Assay(modification).
| Device ID | K954626 |
| 510k Number | K954626 |
| Device Name: | CEDIA DAU BENZODIAZEPINE ASSAY(MODIFICATION) |
| Classification | Enzyme Immunoassay, Benzodiazepine |
| Applicant | MICROGENICS CORP. 2400 BISSO LN. Concord, CA 94520 |
| Contact | Patricia Klimley |
| Correspondent | Patricia Klimley MICROGENICS CORP. 2400 BISSO LN. Concord, CA 94520 |
| Product Code | JXM |
| CFR Regulation Number | 862.3170 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-10-03 |
| Decision Date | 1995-11-27 |