K963517 is an FDA 510(k) clearance for the SPECTRA SCIENCE BIOPSY FORCEPS, a Forceps, Biopsy, Non-electric (Class I — General Controls, product code FCL), submitted by Spectrascience, Inc. (Minnetonka, US). The FDA issued a Cleared decision on December 2, 1996, 90 days after receiving the submission on September 3, 1996. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1075.
| 510(k) Number | K963517 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 03, 1996 |
| Decision Date | December 02, 1996 |
| Days to Decision | 90 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | FCL — Forceps, Biopsy, Non-electric |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 876.1075 |