510(k) K970879 ยท LOS
CARDIOVIT CS-200
| Applicant | Schiller America, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, Jun 25, 1997 |
| Received | Mar 10, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970879
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.