510(k) K905053 ยท IOQ Bed, Flotation Therapy, Powered
STAGE ZERO AIR FLOTATION BED
| Applicant | Lake Medical Products, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Nov 26, 1990 |
| Received | Nov 8, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905053
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.