Submission Details
| 510(k) Number | K863051 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 12, 1986 |
| Decision Date | September 09, 1986 |
| Days to Decision | 28 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
K863051 is an FDA 510(k) clearance for the ALP S.C.E., a Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes (Class II — Special Controls, product code CJE), submitted by J. D. Assoc. (Montclair, US). The FDA issued a Cleared decision on September 9, 1986, 28 days after receiving the submission on August 12, 1986. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1050.
| 510(k) Number | K863051 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 12, 1986 |
| Decision Date | September 09, 1986 |
| Days to Decision | 28 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | CJE — Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 862.1050 |