510(k) K903529 ยท LQC Lithotriptor, Biliary Mechanical
BML SERIES
| Applicant | Olympus Corp., Lake Success NY, US |
| Decision | Substantially Equivalent, Jan 23, 1991 |
| Received | Aug 6, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903529
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 31, 2007 | Olympus America Inc. Olympus Single Use Mechanical Lithotriptor, Model Number BML-V232QR-26, Olympus America, Inc. Terminated |
LQC | None listed |
| Oct 31, 2007 | Olympus America Inc. Olympus Single Use Mechanical Lithotriptor, Model number BML-V232QR-30, Olympus America, Inc. Terminated |
LQC | None listed |
| Oct 31, 2007 | Olympus America Inc. Olympus Single Use Mechanical Lithotriptor, Model number BML-V242QR-30, Olympus America, Inc. Terminated |
LQC | None listed |
| Oct 31, 2007 | Olympus America Inc. Olympus Single Use Mechanical Lithotriptor, Model number BML-201Q, Olympus America, Inc. Terminated |
LQC | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.