510(k) K810543 ยท INX Bed, Air Fluidized
NEO-WAVE SYSTEM
| Applicant | Gaymar Industries, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 6, 1981 |
| Received | Feb 27, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810543
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.