510(k) K850337 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
CARDIAC CATHETERIZATION PACK
| Applicant | Marwood Medical, Inc., Greensboro NC, US |
| Decision | Substantially Equivalent, Feb 25, 1985 |
| Received | Jan 28, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850337
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.