510(k) K090485 ยท LQR Dislodger, Stone, Biliary
COAXIAL ACCORDION ERCP DEVICE, MODELS C0AC19001, COAC20005, COAC22003
| Applicant | Percutaneous Systems, Incorporated, Palo Alto CA, US |
| Decision | Substantially Equivalent, Jul 22, 2009 |
| Received | Feb 25, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090485
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.