The following data is part of a premarket notification filed by Diagnostic Chemicals, Ltd. (usa) with the FDA for Model 303-42/303-43 Aspartate Aminotransferase Kit.
Device ID | K862832 |
510k Number | K862832 |
Device Name: | MODEL 303-42/303-43 ASPARTATE AMINOTRANSFERASE KIT |
Classification | Nadh Oxidation/nad Reduction, Ast/sgot |
Applicant | DIAGNOSTIC CHEMICALS, LTD. (USA) 16 FIRST ST. WEST ROYALTY INDUSTRIAL PARK Charlottestown,pei,canada, CA C1e 1b0 |
Contact | Callbeck, R.t. |
Correspondent | Callbeck, R.t. DIAGNOSTIC CHEMICALS, LTD. (USA) 16 FIRST ST. WEST ROYALTY INDUSTRIAL PARK Charlottestown,pei,canada, CA C1e 1b0 |
Product Code | CIT |
CFR Regulation Number | 862.1100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-07-25 |
Decision Date | 1986-08-12 |