510(k) K880486 ยท IOQ Bed, Flotation Therapy, Powered
DERMGARD SYSTEM 800 AND 900
| Applicant | Dermgard, Inc., New York NY, US |
| Decision | Substantially Equivalent, Feb 22, 1988 |
| Received | Feb 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880486
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.