510(k) K922173 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
MODEL # 830 ST ADULT STIMULATION PADS (STERILE)
| Applicant | Cardiotronics, Inc., West Carlsbad CA, US |
| Decision | Substantially Equivalent, Jun 11, 1992 |
| Received | May 8, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922173
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.