Submission Details
| 510(k) Number | K952768 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 14, 1995 |
| Decision Date | August 24, 1995 |
| Days to Decision | 71 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
K952768 is an FDA 510(k) clearance for the ALKPHASE-B ASSAY KIT, a Electrophoretic Separation, Alkaline Phosphatase Isoenzymes (Class II — Special Controls, product code CIN), submitted by Metra Biosystems, Inc. (Laurel, US). The FDA issued a Cleared decision on August 24, 1995, 71 days after receiving the submission on June 14, 1995. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1050.
| 510(k) Number | K952768 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 14, 1995 |
| Decision Date | August 24, 1995 |
| Days to Decision | 71 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | CIN — Electrophoretic Separation, Alkaline Phosphatase Isoenzymes |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 862.1050 |