510(k) K970363 ยท IOQ Bed, Flotation Therapy, Powered
HYDROTEC LOW AIR LOSS THERAPY BED
| Applicant | Apex Metal, Inc., Los Angeles CA, US |
| Decision | Substantially Equivalent, Nov 17, 1997 |
| Received | Jan 31, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970363
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.