510(k) K983232 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
PADTAK PEDIATRIC DEFIB/CARDIOVERT/PACE/MONITOR-RADIOTRANSPARENT (2X2.25),MODEL 2602, PADTAK PEDIATRIC DEFIB/CARDIOVERT
| Applicant | Tz Medical, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Sep 15, 1999 |
| Received | Sep 14, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983232
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.