510(k) K834352 ยท DRA Catheter, Steerable
ADULT VENT CATHETER
| Applicant | Dlp, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jan 27, 1984 |
| Received | Dec 13, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834352
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 24, 2021 | Medtronic Perfusion Systems DLP Left Heart Vent Catheters, 16 FR. Sterile, Rx Only Open, Classified |
DRA | None listed |
| Aug 24, 2021 | Medtronic Perfusion Systems DLP Left Heart Vent Catheters, 18 FR. Sterile, Rx Only Open, Classified |
DRA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.