K760459 is an FDA 510(k) clearance for the MUELLER HINTON AGAR W/HEMOGLOBIN. This device is classified as a Culture Media, Non-selective And Non-differential (Class I - General Controls, product code JSG).
Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Washington, US). The FDA issued a Cleared decision on September 3, 1976, 17 days after receiving the submission on August 17, 1976.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.2300.
| 510(k) Number | K760459 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 17, 1976 |
| Decision Date | September 03, 1976 |
| Days to Decision | 17 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | — |
| Product Code | JSG — Culture Media, Non-selective And Non-differential |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.2300 |