510(k) K900130 ยท DSB Plethysmograph, Impedance
MODIFIED SEISMOCARDIOGRAPH
| Applicant | Seismed Instruments, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 28, 1990 |
| Received | Jan 5, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900130
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.