K761359 is an FDA 510(k) clearance for the NEOMYCIN AGAR WITH 5% SHEEP BLOOD. This device is classified as a Culture Media, Selective And Non-differential (Class I - General Controls, product code JSJ).
Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Washington, US). The FDA issued a Cleared decision on January 14, 1977, 16 days after receiving the submission on December 29, 1976.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.2360.
| 510(k) Number | K761359 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 29, 1976 |
| Decision Date | January 14, 1977 |
| Days to Decision | 16 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | — |
| Product Code | JSJ — Culture Media, Selective And Non-differential |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.2360 |