510(k) K822084 ยท HIB Speculum, Vaginal, Nonmetal
PRO-SPEC
| Applicant | Exitec, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 19, 1982 |
| Received | Jul 13, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822084
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.