K953452 is an FDA 510(k) clearance for the KETOREX C SANWA. This device is classified as a Acid, Alpha-ketobutyric And Nadh (u.v.), Hydroxybutyric Dehydrogenase (Class I - General Controls, product code JMK).
Submitted by Ihara Medics U.S., Inc. (Valencia, US). The FDA issued a Cleared decision on May 2, 1996, 289 days after receiving the submission on July 18, 1995.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1380.
| 510(k) Number | K953452 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 18, 1995 |
| Decision Date | May 02, 1996 |
| Days to Decision | 289 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Statement |
| Product Code | JMK — Acid, Alpha-ketobutyric And Nadh (u.v.), Hydroxybutyric Dehydrogenase |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1380 |