510(k) K822596 ยท DQO Catheter, Intravascular, Diagnostic
VERTEX PERCUTANEOUS PUNCTURE NEEDLE
| Applicant | Vertex Medical Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 21, 1982 |
| Received | Aug 27, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822596
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.