510(k) K920235 ยท FEO Lithotriptor, Ultrasonic
ULTRASOUND GENERATOR MODLE 2270
| Applicant | Richard Wolf Medical Instruments Corp., Vernon Hills IL, US |
| Decision | Substantially Equivalent, Dec 7, 1992 |
| Received | Jan 17, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920235
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.