The following data is part of a premarket notification filed by Verichem Laboratories, Inc. with the FDA for Hdl-cholesterol Standard, Modification.
| Device ID | K924904 |
| 510k Number | K924904 |
| Device Name: | HDL-CHOLESTEROL STANDARD, MODIFICATION |
| Classification | Calibrator, Primary |
| Applicant | VERICHEM LABORATORIES, INC. 90 NARRAGANSETT AVE. Providence, RI 02907 |
| Contact | Anthony J Dimonte |
| Correspondent | Anthony J Dimonte VERICHEM LABORATORIES, INC. 90 NARRAGANSETT AVE. Providence, RI 02907 |
| Product Code | JIS |
| CFR Regulation Number | 862.1150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-09-29 |
| Decision Date | 1993-01-13 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00852553007230 | K924904 | 000 |
| 00852553007186 | K924904 | 000 |
| 00852553007124 | K924904 | 000 |
| 00852553007025 | K924904 | 000 |