510(k) K882235 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
POLY-TAC
| Applicant | Cardiovascular Group, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Oct 5, 1988 |
| Received | May 27, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882235
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.