510(k) K952345 ยท DQY Catheter, Percutaneous
MEDI-TECH PLATFORM GUIDE CATHETER
| Applicant | Medi-Tech, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Aug 17, 1995 |
| Received | May 19, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952345
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.