510(k) K875137 ยท HES Insufflator, Carbon-Dioxide, Uterotubal (And Accessories)
LAPAROFLATOR 3000, STANDARD AND ELECTRONIC
| Applicant | F.M. Wiest USA, Inc., Cherry Hill NJ, US |
| Decision | Substantially Equivalent, Mar 2, 1988 |
| Received | Dec 15, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875137
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.