510(k) K881825 ยท DYB Introducer, Catheter
MODELS SP5825/SP5835/SP5845/SP5855 PERCU. SHEATH
| Applicant | Spectramed, Inc., Oxnard CA, US |
| Decision | Substantially Equivalent, Sep 28, 1988 |
| Received | Apr 29, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881825
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.