K760589 is an FDA 510(k) clearance for the VCA INHIBITOR. This device is classified as a Supplement, Culture Media (Class I - General Controls, product code JSK).
Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Washington, US). The FDA issued a Cleared decision on October 7, 1976, 34 days after receiving the submission on September 3, 1976.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.2450.
| 510(k) Number | K760589 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 03, 1976 |
| Decision Date | October 07, 1976 |
| Days to Decision | 34 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | — |
| Product Code | JSK — Supplement, Culture Media |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.2450 |