Clearance Summary
Radial Jaw 4 Pulmonary Biopsy Forceps received FDA 510(k) clearance under submission number K252921, sponsored by Boston Scientific Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2025-09-26.
- Submission: K252921
- Applicant / Sponsor: Boston Scientific Corporation
- Clearance pathway: Special
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.4680
- Decision date: 2025-09-26
Classification & Regulation
This clearance is catalogued under FDA product code BWH and 21 CFR 874.4680, within the Ear, Nose, Throat review panel as a Class II device.