The following data is part of a premarket notification filed by Diagnostic Reagents, Inc. with the FDA for Vancomycin Eia Assay.
Device ID | K983280 |
510k Number | K983280 |
Device Name: | VANCOMYCIN EIA ASSAY |
Classification | Radioimmunoassay, Vancomycin |
Applicant | DIAGNOSTIC REAGENTS, INC. 601 CALIFORNIA AVE. Sunnyvale, CA 94086 |
Contact | Yuh-geng Tsay |
Correspondent | Yuh-geng Tsay DIAGNOSTIC REAGENTS, INC. 601 CALIFORNIA AVE. Sunnyvale, CA 94086 |
Product Code | LEH |
CFR Regulation Number | 862.3950 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-09-18 |
Decision Date | 1998-11-06 |