510(k) K880196 ยท HDY Dilator, Cervical, Hygroscopic-Laminaria
LAMINARIA
| Applicant | Medgyn Products, Inc., Downers Grove IL, US |
| Decision | Substantially Equivalent, May 6, 1988 |
| Received | Jan 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880196
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.