Submission Details
| 510(k) Number | K923002 FDA.gov |
| FDA Decision | Cleared SESK |
| Date Received | June 22, 1992 |
| Decision Date | June 28, 1994 |
| Days to Decision | 736 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Statement |
K923002 is an FDA 510(k) clearance for the ENTEROCLYSIS TUBE, a Tubes, Gastrointestinal (and Accessories) (Class II — Special Controls, product code KNT), submitted by Biosearch Medical Products, Inc. (Somerville, US). The FDA issued a Cleared decision on June 28, 1994, 736 days after receiving the submission on June 22, 1992. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5980.
| 510(k) Number | K923002 FDA.gov |
| FDA Decision | Cleared SESK |
| Date Received | June 22, 1992 |
| Decision Date | June 28, 1994 |
| Days to Decision | 736 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Statement |
| Product Code | KNT — Tubes, Gastrointestinal (and Accessories) |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.5980 |