510(k) K882338 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
MODEL #716 ADULT STIM. PADS LOW IMPEDANCE GEL TYPE
| Applicant | Cardiotronics, Inc., West Carlsbad CA, US |
| Decision | Substantially Equivalent, Aug 30, 1988 |
| Received | Jun 6, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882338
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.