Submission Details
| 510(k) Number | K850934 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 07, 1985 |
| Decision Date | June 25, 1985 |
| Days to Decision | 110 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
K850934 is an FDA 510(k) clearance for the PHOSPHORUS, a Phosphomolybdate (colorimetric), Inorganic Phosphorus (Class I — General Controls, product code CEO), submitted by Dilab, Inc. (Miami, US). The FDA issued a Cleared decision on June 25, 1985, 110 days after receiving the submission on March 7, 1985. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1580.
| 510(k) Number | K850934 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 07, 1985 |
| Decision Date | June 25, 1985 |
| Days to Decision | 110 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | CEO — Phosphomolybdate (colorimetric), Inorganic Phosphorus |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 862.1580 |