510(k) K061721 ยท NZD Stretcher, Patient Restraint
PEDI-SPIDER STRAP
| Applicant | Emergency Products and Research, Kent OH, US |
| Decision | Substantially Equivalent, Aug 17, 2006 |
| Received | Jun 19, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061721
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.