510(k) K852097 ยท DTK Filter, Intravascular, Cardiovascular
PERCUTANEOUS GREENFIELD VENA CAVA FILTER SYSTEM
| Applicant | Medi-Tech, Inc., Watertown MA, US |
| Decision | Substantially Equivalent, Nov 1, 1985 |
| Received | May 15, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852097
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.