K834002 is an FDA 510(k) clearance for the LYSINE IRON AGAR. This device is classified as a Culture Media, Multiple Biochemical Test (Class I - General Controls, product code JSE).
Submitted by Micro Media Laboratories (Mchenry, US). The FDA issued a Cleared decision on December 22, 1983, 31 days after receiving the submission on November 21, 1983.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.2320.
| 510(k) Number | K834002 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 21, 1983 |
| Decision Date | December 22, 1983 |
| Days to Decision | 31 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | — |
| Product Code | JSE — Culture Media, Multiple Biochemical Test |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.2320 |