510(k) K821314 ยท KDP Regulator, Vacuum
FEVER METER
| Applicant | Steridyne Corp., Walker MI, US |
| Decision | Substantially Equivalent, May 28, 1982 |
| Received | May 4, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821314
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.