510(k) K870681 ยท FNM Mattress, Air Flotation, Alternating Pressure
HUNTLEIGH BETA II HM85
| Applicant | Huntleigh Technology, Inc., Manalapan NJ, US |
| Decision | Substantially Equivalent, Mar 4, 1987 |
| Received | Feb 19, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870681
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.