510(k) K953923 ยท KNW Instrument, Biopsy
URESIL INTRODUCING NEEDLE
| Applicant | Uresil Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Sep 8, 1995 |
| Received | Aug 18, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953923
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.