The following data is part of a premarket notification filed by Syntron Bioresearch, Inc. with the FDA for Quikstrip One Step Cocaine Assay (cocaine And Cocaine Metabolite Test System.
Device ID | K992207 |
510k Number | K992207 |
Device Name: | QUIKSTRIP ONE STEP COCAINE ASSAY (COCAINE AND COCAINE METABOLITE TEST SYSTEM |
Classification | Enzyme Immunoassay, Cocaine And Cocaine Metabolites |
Applicant | SYNTRON BIORESEARCH, INC. 1420 LOS ANGELES AVE. SUITE 201 Simi Valley, CA 93065 |
Contact | Cleve W Laird |
Correspondent | James M Barquest CALIFORNIA DEPARTMENT OF HEALTH SERVICES P.O. BOX 942732 (MS-357) Sacramento, CA 94234 -7320 |
Product Code | DIO |
CFR Regulation Number | 862.3250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 1999-06-30 |
Decision Date | 1999-07-22 |
Summary: | summary |