510(k) K203630 ยท ODC Endoscope Channel Accessory
BioGuard Air/Water and Suction Valves
| Applicant | Steris Corporations, Mentor OH, US |
| Decision | Substantially Equivalent, Jan 8, 2021 |
| Received | Dec 11, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K203630
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.