510(k) K001969 ยท DQY Catheter, Percutaneous
GT2 FUSION GUIDE WIRE, MODEL NTLHLJ180,NTLHLS180, NTLHLJ300, NTLHLS300
| Applicant | Medtronic Vascular, Danvers MA, US |
| Decision | Substantially Equivalent, Aug 16, 2000 |
| Received | Jun 28, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001969
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.