K925559 is an FDA 510(k) clearance for the BILIARY STONE DISLODGER, a Dislodger, Stone, Biliary (Class II — Special Controls, product code LQR), submitted by Annex Medical, Inc. (Eden Prairie, US). The FDA issued a Cleared decision on December 17, 1992, 44 days after receiving the submission on November 3, 1992. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5010.
| 510(k) Number | K925559 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 03, 1992 |
| Decision Date | December 17, 1992 |
| Days to Decision | 44 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | LQR — Dislodger, Stone, Biliary |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.5010 |