The following data is part of a premarket notification filed by Diagnostic Reagents, Inc. with the FDA for Methadone Metabolite Eia Assay.
Device ID | K931780 |
510k Number | K931780 |
Device Name: | METHADONE METABOLITE EIA ASSAY |
Classification | Enzyme Immunoassay, Methadone |
Applicant | DIAGNOSTIC REAGENTS, INC. 110 PIONEER WAY Mountain View, CA 94041 |
Contact | Yuh-geng Tsay |
Correspondent | Yuh-geng Tsay DIAGNOSTIC REAGENTS, INC. 110 PIONEER WAY Mountain View, CA 94041 |
Product Code | DJR |
CFR Regulation Number | 862.3620 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-04-09 |
Decision Date | 1993-08-23 |