510(k) K792458 ยท DRM Compressor, Cardiac, External
PNEUPAC TEST SET, PT.#500-A250
| Applicant | Pneupac , Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 5, 1980 |
| Received | Dec 3, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792458
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.