K930718 is an FDA 510(k) clearance for the INDOLE SPOT & INDOLE KOVACS REAGENT. This device is classified as a Discs, Strips And Reagents, Microorganism Differentiation (Class I - General Controls, product code JTO).
Submitted by Hardy Diagnostics (Santa Maria, US). The FDA issued a Cleared decision on April 23, 1993, 71 days after receiving the submission on February 11, 1993.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.2660.
| 510(k) Number | K930718 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 11, 1993 |
| Decision Date | April 23, 1993 |
| Days to Decision | 71 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | Statement |
| Product Code | JTO — Discs, Strips And Reagents, Microorganism Differentiation |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.2660 |