510(k) K833726 ยท HXS Twister, Wire
KLEIN WIRE TIGHTENER/BIONIC WIRE
| Applicant | Bionic Instrument Corp., Walker MI, US |
| Decision | Substantially Equivalent, Dec 22, 1983 |
| Received | Oct 24, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833726
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.