K252722
- 510(k) number
- K252722
- Device name
- Biopsy Forceps
- Applicant
- Fehling Instruments GmbH DE
- Product code
- DWZ — Device, Biopsy, Endomyocardial
- Decision date
- 2025-09-30
- Date received
- 2025-08-28
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K252722.pdf
Official FDA record: K252722
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.