The following data is part of a premarket notification filed by Roche Diagnostic Systems, Inc. with the FDA for Roche Unimate Fructosamine Reagent.
| Device ID | K961674 |
| 510k Number | K961674 |
| Device Name: | ROCHE UNIMATE FRUCTOSAMINE REAGENT |
| Classification | Assay, Glycosylated Hemoglobin |
| Applicant | ROCHE DIAGNOSTIC SYSTEMS, INC. BRANCHBURG TOWNSHIP 1080 U.S. HIGHWAY 202 Somerville, NJ 08876 -3771 |
| Contact | Maria Feijoo |
| Correspondent | Maria Feijoo ROCHE DIAGNOSTIC SYSTEMS, INC. BRANCHBURG TOWNSHIP 1080 U.S. HIGHWAY 202 Somerville, NJ 08876 -3771 |
| Product Code | LCP |
| CFR Regulation Number | 864.7470 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-05-01 |
| Decision Date | 1996-09-27 |