510(k) K950318 ยท CBH Device, Fixation, Tracheal Tube
FLEX BLUE
| Applicant | King Systems Corp., Noblesville IN, US |
| Decision | Substantially Equivalent, Feb 13, 1995 |
| Received | Jan 26, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950318
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.