510(k) K880575 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
CARDIOLIFE TEC-7300 W/OPTIONAL ACCESSORIES
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Aug 2, 1988 |
| Received | Feb 10, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880575
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.