510(k) K933004 ยท FNM Mattress, Air Flotation, Alternating Pressure
PEGASUS BIWAVE SYSTEM
| Applicant | Pegasus Airwave, Inc., Deerfield Beach FL, US |
| Decision | Substantially Equivalent, Mar 7, 1994 |
| Received | Jun 21, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933004
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.