510(k) K940178 ยท DSP System, Balloon, Intra-Aortic And Control
PERCOR STAT-DL 9.5 FR.34CC & 40CC /PERCOR STAT-DL 10.5 FR.40CC & 50CC INTRA-AORTIC BALLOON MODIFICATION
| Applicant | Datascope Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Aug 9, 1994 |
| Received | Jan 12, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940178
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.