Submission Details
| 510(k) Number | K914025 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 09, 1991 |
| Decision Date | November 22, 1991 |
| Days to Decision | 74 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Statement |
K914025 is an FDA 510(k) clearance for the TECHNICON AXON(TM) SYSTEMS, ALT(P 5-P)/AST(P 5-P), a Nadh Oxidation/nad Reduction, Ast/sgot (Class II — Special Controls, product code CIT), submitted by Technicon Instruments Corp. (New York, US). The FDA issued a Cleared decision on November 22, 1991, 74 days after receiving the submission on September 9, 1991. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1100.
| 510(k) Number | K914025 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 09, 1991 |
| Decision Date | November 22, 1991 |
| Days to Decision | 74 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Statement |
| Product Code | CIT — Nadh Oxidation/nad Reduction, Ast/sgot |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 862.1100 |