510(k) K021999 ยท FPA Set, Administration, Intravascular
GRIPPER PLUS NEEDLE
| Applicant | Deltec, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Aug 13, 2002 |
| Received | Jun 19, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021999
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 15, 2019 | Centurion Medical Products Corporation Port full Access Tray
Product Code: DT19330 Terminated |
LRP | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.