510(k) K102887 ยท FFL Dislodger, Stone, Basket, Ureteral, Metal
ACCORDION STONE MANAGEMENT DEVICE MODEL AC281205 AND AC3814510
| Applicant | Percutaneous Systems, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, May 16, 2011 |
| Received | Sep 30, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102887
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.