510(k) K903917 ยท DSP System, Balloon, Intra-Aortic And Control
COMPACT MONITOR SMK 210,211,230,231,240
| Applicant | Ppg Hellige B.V., West Germany, DE |
| Decision | Substantially Equivalent, Jan 18, 1991 |
| Received | Aug 24, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903917
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.