K060953 is an FDA 510(k) clearance for the OCCULTECH FECAL OCCULT BLOOD RAPID TEST. This device is classified as a Reagent, Occult Blood (Class II - Special Controls, product code KHE).
Submitted by Yd Diagnostics Corp. (Annandale, US). The FDA issued a Cleared decision on September 18, 2006, 165 days after receiving the submission on April 6, 2006.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.6550.
| 510(k) Number | K060953 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 06, 2006 |
| Decision Date | September 18, 2006 |
| Days to Decision | 165 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | Summary PDF |
| Product Code | KHE — Reagent, Occult Blood |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 864.6550 |