K822739 is an FDA 510(k) clearance for the AHBD. This device is classified as a Acid, Alpha-ketobutyric And Nadh (u.v.), Hydroxybutyric Dehydrogenase (Class I - General Controls, product code JMK).
Submitted by Gilford Diagnostics (Mchenry, US). The FDA issued a Cleared decision on October 18, 1982, 39 days after receiving the submission on September 9, 1982.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1380.
| 510(k) Number | K822739 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 09, 1982 |
| Decision Date | October 18, 1982 |
| Days to Decision | 39 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | JMK — Acid, Alpha-ketobutyric And Nadh (u.v.), Hydroxybutyric Dehydrogenase |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1380 |