The following data is part of a premarket notification filed by Diagnostic Chemicals, Ltd. (usa) with the FDA for Glucose Hk-60 Assay Kit Cat. #201-39.
Device ID | K860625 |
510k Number | K860625 |
Device Name: | GLUCOSE HK-60 ASSAY KIT CAT. #201-39 |
Classification | Hexokinase, Glucose |
Applicant | DIAGNOSTIC CHEMICALS, LTD. (USA) 435 MAIN ST. Monroe, CT 06468 |
Contact | Karen Callbeck |
Correspondent | Karen Callbeck DIAGNOSTIC CHEMICALS, LTD. (USA) 435 MAIN ST. Monroe, CT 06468 |
Product Code | CFR |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-02-19 |
Decision Date | 1986-03-17 |