ClearanceBrief
510(k) K210651 ยท FAS Electrode, Electrosurgical, Active, Urological

Resection Electrodes with HF cable

ApplicantOlympus Winter & Ibe GmbH, Hamburg, DE
DecisionSubstantially Equivalent, Aug 3, 2021
ReceivedMar 4, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K210651

DateFirm and productCodeLinked 510(k)
Feb 20, 2026Olympus Corporation of the Americas
Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological applications.
Open, Classified
HIHNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.