510(k) K930548 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
DPD DEFIBRILLATOR
| Applicant | Medical Research Laboratories, Inc., Buffalo Grove IL, US |
| Decision | Substantially Equivalent, Jun 25, 1993 |
| Received | Feb 3, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930548
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.