The following data is part of a premarket notification filed by Microgenics Corp. with the FDA for Cedia Vitamin B12 (no Boil) Assay.
| Device ID | K951134 |
| 510k Number | K951134 |
| Device Name: | CEDIA VITAMIN B12 (NO BOIL) ASSAY |
| Classification | Radioassay, Vitamin B12 |
| 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 | CDD |
| CFR Regulation Number | 862.1810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-03-13 |
| Decision Date | 1995-07-11 |