510(k) K892323 ยท DSB Plethysmograph, Impedance
SEISMOCARDIOGRAPH - SCG(TM) 1000 SERIES
| Applicant | Seismed Instruments, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 30, 1989 |
| Received | Apr 6, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892323
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.