510(k) K041917 ยท BTR Tube, Tracheal (W/Wo Connector)
PLASIATEK ACTUATOR
| Applicant | Plasiatek, LLC, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jan 7, 2005 |
| Received | Jul 16, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041917
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.