K120591 is an FDA 510(k) clearance for the DIAMOND TOKYO BOEKI ISE MODULE CALIBRATOR 1,2,1-2. This device is classified as a Calibrator, Secondary (Class II - Special Controls, product code JIT).
Submitted by Diamond Diagnostics, Inc. (Holliston, US). The FDA issued a Cleared decision on April 17, 2012, 49 days after receiving the submission on February 28, 2012.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1150.
| 510(k) Number | K120591 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 28, 2012 |
| Decision Date | April 17, 2012 |
| Days to Decision | 49 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | JIT - Calibrator, Secondary |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1150 |