510(k) K900236 ยท CBH Device, Fixation, Tracheal Tube
ET-RESTRAINT CAT. # ER 4000
| Applicant | Ventlab Corp., Hackensack NJ, US |
| Decision | Substantially Equivalent, Feb 2, 1990 |
| Received | Jan 17, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900236
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.