510(k) K952085 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
DPD DEFIBRILLATOR
| Applicant | Medical Research Laboratories, Inc., Buffalo Grove IL, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Jun 5, 1995 |
| Received | May 3, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952085
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.