K963794 is an FDA 510(k) clearance for the PUNCTURENEEDLE. This device is classified as a Instrument, Biopsy (Class II - Special Controls, product code KNW).
Submitted by Ferguson Medical (Chico, US). The FDA issued a Cleared decision on March 19, 1998, 545 days after receiving the submission on September 20, 1996.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1075.
| 510(k) Number | K963794 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 20, 1996 |
| Decision Date | March 19, 1998 |
| Days to Decision | 545 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | KNW — Instrument, Biopsy |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.1075 |