510(k) K101885 ยท DQY Catheter, Percutaneous
MEDTRONIC C315 DELIVERY CATHETER
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Sep 9, 2010 |
| Received | Jul 6, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101885
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 9, 2021 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) C315-HIS Delivery Catheter Open, Classified |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.