510(k) K903539 ยท CBH Device, Fixation, Tracheal Tube
SALTER LABS MODEL #1015
| Applicant | Salter Labs, Arvin CA, US |
| Decision | Substantially Equivalent, Dec 17, 1990 |
| Received | Aug 7, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903539
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.