K252921
- 510(k) number
- K252921
- Device name
- Radial Jaw 4 Pulmonary Biopsy Forceps
- Applicant
- Boston Scientific Corporation MA · US
- Product code
- BWH — Forceps, Biopsy, Bronchoscope (Non-Rigid)
- Decision date
- 2025-09-26
- Date received
- 2025-09-12
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Ear, Nose, Throat
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K252921.pdf
Official FDA record: K252921
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.