510(k) K833751 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
PORTA PULSE III #D320
| Applicant | Medical Research Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 11, 1984 |
| Received | Oct 26, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833751
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.