K253000
- 510(k) number
- K253000
- Device name
- CryoFreeze Wart and Skin Tag Remover
- Applicant
- Cryosurgery, Inc. TN · US
- Product code
- GEH — Unit, Cryosurgical, Accessories
- Decision date
- 2025-10-16
- Date received
- 2025-09-18
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K253000.pdf
Official FDA record: K253000
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.