510(k) K953675 ยท FNM Mattress, Air Flotation, Alternating Pressure
ALTADYNE
| Applicant | Lumex, Inc., Bay Shore NY, US |
| Decision | Substantially Equivalent, Sep 28, 1995 |
| Received | Aug 7, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953675
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.