510(k) K882329 ยท DXT Injector And Syringe, Angiographic
L-F COILED EXTENSION TUBING
| Applicant | Mallinckrodt Group, Inc., Cincinnati OH, US |
| Decision | Substantially Equivalent, Sep 2, 1988 |
| Received | Jun 6, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882329
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 29, 2012 | Mallinckrodt Inc Coiled 60" Low Pressure Extension Tube 400 PSI Max; packaged in Plastic and Tyvec pouch, with 100 pouches per case; Liebel-Flarsheim Company, Cincinnati, OH 45237. Made in Mexico.
Sterile, The purpos Terminated |
DXT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.