510(k) K962123 ยท FNM Mattress, Air Flotation, Alternating Pressure
AKROTECH 4000T KINETIC TURNING LOW AIR LOSS SYSTEM
| Applicant | Lumex, Inc., Bay Shore NY, US |
| Decision | Substantially Equivalent, Jul 18, 1996 |
| Received | May 31, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962123
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.