510(k) K870045 ยท INX Bed, Air Fluidized
SKYTRON MODEL 610-2
| Applicant | Skytron, Div. the Kmw Group, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Feb 4, 1987 |
| Received | Jan 5, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870045
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.