The following data is part of a premarket notification filed by Advanced Biomedical Methods, Inc. with the FDA for Gluc Opap, In Vitro Diag. For Glucose.
Device ID | K761153 |
510k Number | K761153 |
Device Name: | GLUC OPAP, IN VITRO DIAG. FOR GLUCOSE |
Classification | Glucose Oxidase, Glucose |
Applicant | ADVANCED BIOMEDICAL METHODS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CGA |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1976-11-29 |
Decision Date | 1976-12-09 |