510(k) K974745 ยท DRC Trocar
MANAN GWI GUIDE WIRE INTRODUCER
| Applicant | Medical Device Technologies, Inc., Gainsville FL, US |
| Decision | Substantially Equivalent, Apr 6, 1998 |
| Received | Dec 19, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974745
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 13, 2010 | Medical Device Technologies, Inc. Angiotech Vascular Access Needle.
A) "Modified Potts/Cournand" Needle. STERILE. Product Number: MPCN1802. 510k K974745. Qty Dist. - 425.
B) "Seldinger" Needle. STERILE. Product Number: SN Terminated |
DRC | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.