The following data is part of a premarket notification filed by Sigma Diagnostics, Inc. with the FDA for Kc 40 Micro Coagulation Analyzer System (k3632).
| Device ID | K960875 |
| 510k Number | K960875 |
| Device Name: | KC 40 MICRO COAGULATION ANALYZER SYSTEM (K3632) |
| Classification | System, Multipurpose For In Vitro Coagulation Studies |
| Applicant | SIGMA DIAGNOSTICS, INC. 545 SOUTH EWING AVE. St. Louis, MO 63103 |
| Contact | William R Gilbert, Ph.d. |
| Correspondent | William R Gilbert, Ph.d. SIGMA DIAGNOSTICS, INC. 545 SOUTH EWING AVE. St. Louis, MO 63103 |
| Product Code | JPA |
| CFR Regulation Number | 864.5425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-03-04 |
| Decision Date | 1996-09-10 |
| Summary: | summary |