The following data is part of a premarket notification filed by Microgenics Corp. with the FDA for Cedia Dau Propoxyphene Assay.
| Device ID | K951133 |
| 510k Number | K951133 |
| Device Name: | CEDIA DAU PROPOXYPHENE ASSAY |
| Classification | Enzyme Immunoassay, Propoxyphene |
| Applicant | MICROGENICS CORP. 2380A BISSO LN. Concord, CA 94520 |
| Contact | Mary Koning |
| Correspondent | Mary Koning MICROGENICS CORP. 2380A BISSO LN. Concord, CA 94520 |
| Product Code | JXN |
| CFR Regulation Number | 862.3700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-03-13 |
| Decision Date | 1995-05-02 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00884883004351 | K951133 | 000 |
| 00884883004283 | K951133 | 000 |
| 00884883004221 | K951133 | 000 |