510(k) K923977 ยท IOQ Bed, Flotation Therapy, Powered
AKROTECH 4000
| Applicant | Lumex, Inc., Bay Shore NY, US |
| Decision | Substantially Equivalent, Feb 12, 1993 |
| Received | Aug 7, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923977
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.