The following data is part of a premarket notification filed by Diagnostic Reagents, Inc. with the FDA for Procainamide Enzyme Immunoassay.
Device ID | K962463 |
510k Number | K962463 |
Device Name: | PROCAINAMIDE ENZYME IMMUNOASSAY |
Classification | Enzyme Immunoassay, Procainamide |
Applicant | DIAGNOSTIC REAGENTS, INC. 601 CALIFORNIA AVE. Sunnyvale, CA 94086 |
Contact | Yuh-geng Tsay,ph.d. |
Correspondent | Yuh-geng Tsay,ph.d. DIAGNOSTIC REAGENTS, INC. 601 CALIFORNIA AVE. Sunnyvale, CA 94086 |
Product Code | LAR |
CFR Regulation Number | 862.3320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-06-25 |
Decision Date | 1996-08-14 |