The following data is part of a premarket notification filed by Roche Diagnostic Systems, Inc. with the FDA for Roche Unimate Hdl Direct Reagen (with Pol Claim).
| Device ID | K973369 |
| 510k Number | K973369 |
| Device Name: | ROCHE UNIMATE HDL DIRECT REAGEN (WITH POL CLAIM) |
| Classification | Ldl & Vldl Precipitation, Hdl |
| Applicant | ROCHE DIAGNOSTIC SYSTEMS, INC. BRANCHBURG TOWNSHIP 1080 U.S. HIGHWAY 202 Somerville, NJ 08876 -3771 |
| Contact | James W Haynes |
| Correspondent | James W Haynes ROCHE DIAGNOSTIC SYSTEMS, INC. BRANCHBURG TOWNSHIP 1080 U.S. HIGHWAY 202 Somerville, NJ 08876 -3771 |
| Product Code | LBR |
| CFR Regulation Number | 862.1475 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-09-08 |
| Decision Date | 1997-11-21 |
| Summary: | summary |