510(k) K823517 ยท HGD Applicator, Vaginal
THE KLINE APPLICATOR
| Applicant | Kline Technologies, Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 18, 1983 |
| Received | Nov 29, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823517
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.