510(k) K823828 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
THERACARD 400
| Applicant | Siemens Medical Solutions USA, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Mar 17, 1983 |
| Received | Dec 20, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823828
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.