Submission Details
| 510(k) Number | K031545 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | May 16, 2003 |
| Decision Date | July 16, 2003 |
| Days to Decision | 61 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | Statement |
K031545 is an FDA 510(k) clearance for the SENSITITRE 18-24 HOUR SUSCEPTIBILITY PLATE, a Manual Antimicrobial Susceptibility Test Systems (Class II — Special Controls, product code JWY), submitted by Trek Diagnostic Systems, Inc. (Cleveland, US). The FDA issued a Cleared decision on July 16, 2003, 61 days after receiving the submission on May 16, 2003. This device falls under the Microbiology review panel. Regulated under 21 CFR 866.1640.
| 510(k) Number | K031545 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | May 16, 2003 |
| Decision Date | July 16, 2003 |
| Days to Decision | 61 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | Statement |
| Product Code | JWY — Manual Antimicrobial Susceptibility Test Systems |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 866.1640 |