510(k) K962778 ยท FMQ Restraint, Protective
THE L-BOW ARM RESTRAINT
| Applicant | Heelbo, Inc., Libertyville IL, US |
| Decision | Substantially Equivalent, Oct 9, 1996 |
| Received | Jul 17, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962778
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.