K821771 is an FDA 510(k) clearance for the MACRO-VUE CARD TEST, AMIKACIN. This device is classified as a Radioimmunoassay, Amikacin (Class II - Special Controls, product code KLQ).
Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Washington, US). The FDA issued a Cleared decision on June 25, 1982, 9 days after receiving the submission on June 16, 1982.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3035.
| 510(k) Number | K821771 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 16, 1982 |
| Decision Date | June 25, 1982 |
| Days to Decision | 9 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
| Product Code | KLQ — Radioimmunoassay, Amikacin |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3035 |