510(k) K883121 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
QUIK-PACE II ELECTRODES
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Sep 20, 1988 |
| Received | Jul 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883121
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.