510(k) K890012 ยท FNM Mattress, Air Flotation, Alternating Pressure
HUNTLEIGH DYNAMIC FLOTATION SYSTEM
| Applicant | Huntleigh Technology, Inc., Manalapan NJ, US |
| Decision | Substantially Equivalent, Mar 29, 1989 |
| Received | Jan 3, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890012
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.