510(k) K022099 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
SAFE-T-PEEL SAFETY NEEDLE/INTRODUCER, MODELS 350-300 S, 360-300'S,380-300'S,390-300'S
| Applicant | Hdc Corp., Washington DC, US |
| Decision | Substantially Equivalent, Sep 20, 2002 |
| Received | Jun 27, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022099
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.