The following data is part of a premarket notification filed by Sigma Diagnostics, Inc. with the FDA for Ez Ldl Cholesterol Test System.
| Device ID | K993741 |
| 510k Number | K993741 |
| Device Name: | EZ LDL CHOLESTEROL TEST SYSTEM |
| Classification | System, Test, Low Density, Lipoprotein |
| Applicant | SIGMA DIAGNOSTICS, INC. 545 SOUTH EWING AVE. St. Louis, MO 63103 |
| Contact | William R Gilbert |
| Correspondent | William R Gilbert SIGMA DIAGNOSTICS, INC. 545 SOUTH EWING AVE. St. Louis, MO 63103 |
| Product Code | MRR |
| CFR Regulation Number | 862.1475 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-11-04 |
| Decision Date | 2000-07-03 |
| Summary: | summary |