510(k) K920157 ยท DXY Implantable Pacemaker Pulse-Generator
SCHNEIDER 8 FR. STAMINA(TM) GUIDING CATHETER
| Applicant | Schneider Intl., Ltd., Plymouth MN, US |
| Decision | Substantially Equivalent, Mar 16, 1992 |
| Received | Jan 14, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920157
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.