The following data is part of a premarket notification filed by Diagnostic Reagents, Inc. with the FDA for Benzodiazepine Enzyme Immunoassay.
Device ID | K930529 |
510k Number | K930529 |
Device Name: | BENZODIAZEPINE ENZYME IMMUNOASSAY |
Classification | Enzyme Immunoassay, Benzodiazepine |
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 | JXM |
CFR Regulation Number | 862.3170 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-02-02 |
Decision Date | 1993-08-05 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00380740005580 | K930529 | 000 |