K962269 is an FDA 510(k) clearance for the CEDIA CARDIAC TDM MULTI-CALS. This device is classified as a Calibrator, Multi-analyte Mixture (Class II - Special Controls, product code JIX).
Submitted by Boehringer Mannheim Corp. (Concord, US). The FDA issued a Cleared decision on October 29, 1996, 138 days after receiving the submission on June 13, 1996.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.1150.
| 510(k) Number | K962269 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 13, 1996 |
| Decision Date | October 29, 1996 |
| Days to Decision | 138 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Summary PDF |
| Product Code | JIX — Calibrator, Multi-analyte Mixture |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1150 |