K873360 is an FDA 510(k) clearance for the ENTERON PERCUTAN. ENDOSCOPIC GASTROSTOMY TRAY-PEG. This device is classified as a Tubes, Gastrointestinal (and Accessories) (Class II - Special Controls, product code KNT).
Submitted by Endovations (Camp Hill, US). The FDA issued a Cleared decision on March 30, 1988, 222 days after receiving the submission on August 21, 1987.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5980.
| 510(k) Number | K873360 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 21, 1987 |
| Decision Date | March 30, 1988 |
| Days to Decision | 222 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | — |
| Product Code | KNT — Tubes, Gastrointestinal (and Accessories) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.5980 |