510(k) K921833 ยท FMF Syringe, Piston
ENDOPATH ENDO-SURGERY PERCUTANEOUS CATHETER INTROD
| Applicant | ETHICON, Inc., Cincinnati OH, US |
| Decision | Unknown, Sep 21, 1992 |
| Received | Apr 16, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921833
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.