K955347 is an FDA 510(k) clearance for the ULTRAFLEX. This device is classified as a Prosthesis, Esophageal (Class II - Special Controls, product code ESW).
Submitted by Boston Scientific Corp (Natick,, US). The FDA issued a Cleared decision on February 16, 1996, 87 days after receiving the submission on November 21, 1995.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 878.3610.
| 510(k) Number | K955347 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 21, 1995 |
| Decision Date | February 16, 1996 |
| Days to Decision | 87 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | ESW — Prosthesis, Esophageal |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.3610 |