510(k) K881705 ยท INX Bed, Air Fluidized
MODEL 5000 AIR-FLUIDIZED SUPPORT SYSTEM
| Applicant | Surgi-Med, Inc., Lansing MI, US |
| Decision | Substantially Equivalent, Jul 13, 1988 |
| Received | Apr 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881705
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.