510(k) K911057 ยท INX Bed, Air Fluidized
DERMATEK 4000
| Applicant | Anacom General Corp., Anaheim CA, US |
| Decision | Substantially Equivalent, Apr 5, 1991 |
| Received | Mar 8, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911057
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.