K233347
- 510(k) number
- K233347
- Device name
- Verruca-Freeze® H
- Applicant
- Cryosurgery, Inc. TN · US
- Product code
- GEH — Unit, Cryosurgical, Accessories
- Decision date
- 2023-12-04
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K233347.pdf
Official FDA record: K233347
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.