510(k) K832192 ยท FHN Ligator, Hemorrhoidal
SUCTION-HEMORRHOID-LIGATOR
| Applicant | Research Endoscope Systems Intl., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 27, 1983 |
| Received | Jul 8, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832192
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.