K984608 is an FDA 510(k) clearance for the GENTAMICIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC. This device is classified as a Susceptibility Test Discs, Antimicrobial (Class II - Special Controls, product code JTN).
Submitted by Oxoid , Ltd. (Basingstoke, GB). The FDA issued a Cleared decision on March 9, 1999, 71 days after receiving the submission on December 28, 1998.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.1620.
| 510(k) Number | K984608 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 28, 1998 |
| Decision Date | March 09, 1999 |
| Days to Decision | 71 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | Statement |
| Product Code | JTN — Susceptibility Test Discs, Antimicrobial |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 866.1620 |