The following data is part of a premarket notification filed by Sigma Diagnostics, Inc. with the FDA for Sigma Diagnostics Cx -3 Calibration Standard, Level 2.
| Device ID | K963543 |
| 510k Number | K963543 |
| Device Name: | SIGMA DIAGNOSTICS CX -3 CALIBRATION STANDARD, LEVEL 2 |
| Classification | Calibrator, Multi-analyte Mixture |
| 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 | JIX |
| CFR Regulation Number | 862.1150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-09-04 |
| Decision Date | 1996-10-30 |
| Summary: | summary |