510(k) K030589 ยท DQY Catheter, Percutaneous
MODIFICATION TO NUMED TYSHAK II AND Z-MED II PTV CATHETERS
| Applicant | NuMED, Inc., Hopkinton NY, US |
| Decision | Substantially Equivalent, May 21, 2003 |
| Received | Feb 25, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030589
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.