510(k) K810820 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
CARDIOPULMONARY BYPASS
| Applicant | Dlp, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Apr 3, 1981 |
| Received | Mar 24, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810820
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 10, 2024 | Medtronic Perfusion Systems Medtronic I.M.A. Cannulae: DLP 1 mm Arteriotomy Cannula, Model Number 31001 Open, Classified |
DWF | None listed |
| May 10, 2024 | Medtronic Perfusion Systems Medtronic Vessel Cannulae:
a) DLP 2 mm Vessel Cannula Blunt Tip, Model Number 30004;
b) DLP 3 mm Vessel Cannula Blunt Tip, Model Number 30003 Open, Classified |
DWF | None listed |
| Mar 19, 2024 | Medtronic Perfusion Systems Medtronic DLP Vessel Cannula, Model Number REF 30000 Open, Classified |
DWF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.