The following data is part of a premarket notification filed by Microgenics Corp. with the FDA for Cedia(r) Dau Pcp Assay.
Device ID | K935650 |
510k Number | K935650 |
Device Name: | CEDIA(R) DAU PCP ASSAY |
Classification | Enzyme Immunoassay, Phencyclidine |
Applicant | MICROGENICS CORP. 2380A BISSO LN. Concord, CA 94520 |
Contact | Betsy Soares-maddox |
Correspondent | Betsy Soares-maddox MICROGENICS CORP. 2380A BISSO LN. Concord, CA 94520 |
Product Code | LCM |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-11-23 |
Decision Date | 1994-04-05 |