510(k) K870729 ยท DTK Filter, Intravascular, Cardiovascular
TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER
| Applicant | Medi-Tech, Inc., Watertown MA, US |
| Decision | Substantially Equivalent, Apr 9, 1987 |
| Received | Feb 25, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870729
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.