510(k) K230283 ยท DYB Introducer, Catheter
Peel-Away Introducer (405104, 405108, 405112, 405116, 405118, 405119, 405120, 405122, 405124, 405128, 405129, 405136, 405144, 405145, 405146, 405147, 405149, 405153, 405154, 405254, 405269, 405270, 405404, 405408, 405412, 405416, 405418, 405420, 405422, 405424, 405428)
| Applicant | ABBOTT MEDICAL, Sylmar CA, US |
| Decision | Substantially Equivalent, Mar 1, 2023 |
| Received | Feb 1, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230283
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.