The following data is part of a premarket notification filed by Microgenics Corp. with the FDA for Cedia Dau Amphetamines Assay.
Device ID | K951154 |
510k Number | K951154 |
Device Name: | CEDIA DAU AMPHETAMINES ASSAY |
Classification | Enzyme Immunoassay, Amphetamine |
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 | DKZ |
CFR Regulation Number | 862.3100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-03-14 |
Decision Date | 1995-05-08 |