510(k) K970401 ยท DQY Catheter, Percutaneous
MEDI-DYNE GUIDING CATHETER
| Applicant | Medi-Dyne, Inc., Queensbury NY, US |
| Decision | Substantially Equivalent, Aug 1, 1997 |
| Received | Feb 3, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970401
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.