The following data is part of a premarket notification filed by Em Diagnostic Systems, Inc. with the FDA for Aspartate Aminotransferase Test.
Device ID | K903197 |
510k Number | K903197 |
Device Name: | ASPARTATE AMINOTRANSFERASE TEST |
Classification | Nadh Oxidation/nad Reduction, Ast/sgot |
Applicant | EM DIAGNOSTIC SYSTEMS, INC. 480 DEMOCRAT RD. Gibbstown, NJ 08027 |
Contact | Anna G Bentley |
Correspondent | Anna G Bentley EM DIAGNOSTIC SYSTEMS, INC. 480 DEMOCRAT RD. Gibbstown, NJ 08027 |
Product Code | CIT |
CFR Regulation Number | 862.1100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-07-19 |
Decision Date | 1990-08-17 |