The following data is part of a premarket notification filed by Diagnostic Reagents, Inc. with the FDA for Barbiturate Serum Tox Eia Assay.
Device ID | K960664 |
510k Number | K960664 |
Device Name: | BARBITURATE SERUM TOX EIA ASSAY |
Classification | Enzyme Immunoassay, Barbiturate |
Applicant | DIAGNOSTIC REAGENTS, INC. 601 CALIFORNIA AVE. Sunnyvale, CA 94086 |
Contact | Yug-geng Tsay, Ph.d. |
Correspondent | Yug-geng Tsay, Ph.d. DIAGNOSTIC REAGENTS, INC. 601 CALIFORNIA AVE. Sunnyvale, CA 94086 |
Product Code | DIS |
CFR Regulation Number | 862.3150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-02-16 |
Decision Date | 1996-05-06 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00380740005573 | K960664 | 000 |
00630414526911 | K960664 | 000 |
00884883005587 | K960664 | 000 |