K941256 is an FDA 510(k) clearance for the QUICK CORE II. This device is classified as a Instrument, Biopsy (Class II - Special Controls, product code KNW).
Submitted by Proact, Ltd. (State College, US). The FDA issued a Cleared decision on July 13, 1994, 121 days after receiving the submission on March 14, 1994.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1075.
| 510(k) Number | K941256 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 14, 1994 |
| Decision Date | July 13, 1994 |
| Days to Decision | 121 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Statement |
| Product Code | KNW — Instrument, Biopsy |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.1075 |