The following data is part of a premarket notification filed by American Monitor Corp. with the FDA for Neochrome(r) Iii Glucose.
| Device ID | K892002 |
| 510k Number | K892002 |
| Device Name: | NEOCHROME(R) III GLUCOSE |
| Classification | Glucose Oxidase, Glucose |
| Applicant | AMERICAN MONITOR CORP. P.O. BOX 68505 Indianapolis, IN 46268 |
| Contact | Jennifer Line |
| Correspondent | Jennifer Line AMERICAN MONITOR CORP. P.O. BOX 68505 Indianapolis, IN 46268 |
| Product Code | CGA |
| CFR Regulation Number | 862.1345 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-03-28 |
| Decision Date | 1989-06-12 |