K993554 is an FDA 510(k) clearance for the YEASTEST. This device is classified as a Kit, Identification, Yeast (Class I - General Controls, product code JXB).
Submitted by Diagnostic Markers, Inc. (Irvine, US). The FDA issued a Cleared decision on February 10, 2000, 113 days after receiving the submission on October 20, 1999.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.2660.
| 510(k) Number | K993554 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 20, 1999 |
| Decision Date | February 10, 2000 |
| Days to Decision | 113 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | Statement |
| Product Code | JXB — Kit, Identification, Yeast |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.2660 |