The following data is part of a premarket notification filed by Synermed, Inc. with the FDA for Synermed Hdl Cholestlerol Reagent Kit.
| Device ID | K924427 |
| 510k Number | K924427 |
| Device Name: | SYNERMED HDL CHOLESTLEROL REAGENT KIT |
| Classification | Ldl & Vldl Precipitation, Hdl |
| Applicant | SYNERMED, INC. 1688 50TH AVENUE, MONTREAL (LACHINE), Quebec, Canada, CA H8t 2v5 |
| Contact | Marcia J Arentz |
| Correspondent | Marcia J Arentz SYNERMED, INC. 1688 50TH AVENUE, MONTREAL (LACHINE), Quebec, Canada, CA H8t 2v5 |
| Product Code | LBR |
| CFR Regulation Number | 862.1475 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-09-01 |
| Decision Date | 1992-11-09 |