510(k) K941869 ยท KZF Device, Medical Examination, Ac Powered
SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG
| Applicant | The Lighthouse For the Blind, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Aug 3, 1994 |
| Received | Apr 18, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941869
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.