510(k) K890935 ยท IOQ Bed, Flotation Therapy, Powered
SYSTEM 3000 FLUIDIZED AIR BED
| Applicant | Dermanetics Corp., Long Beach CA, US |
| Decision | Substantially Equivalent, Mar 15, 1989 |
| Received | Feb 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890935
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.