K961897 is an FDA 510(k) clearance for the WILSON-COOK BILIARY INTRODUCER WITH ASPIRATION BIOPSY NEEDLE. This device is classified as a Biopsy Needle (Class II - Special Controls, product code FCG).
Submitted by Wilson-Cook Medical, Inc. (Winston-Salem, US). The FDA issued a Cleared decision on January 29, 1997, 258 days after receiving the submission on May 16, 1996.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1075.
| 510(k) Number | K961897 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 16, 1996 |
| Decision Date | January 29, 1997 |
| Days to Decision | 258 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | FCG — Biopsy Needle |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.1075 |