The following data is part of a premarket notification filed by Orange Medical Instruments, Inc. with the FDA for Beta Scan Reagent Strip.
| Device ID | K832691 |
| 510k Number | K832691 |
| Device Name: | BETA SCAN REAGENT STRIP |
| Classification | Glucose Oxidase, Glucose |
| Applicant | ORANGE MEDICAL INSTRUMENTS, 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 | 1983-08-10 |
| Decision Date | 1983-11-14 |