Clearance Summary
THE FERN CRYOPROBE received FDA 510(k) clearance under submission number K892237, sponsored by Cryogenic Instruments & Equipment , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1989-07-25.
- Submission: K892237
- Applicant / Sponsor: Cryogenic Instruments & Equipment , Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4350
- Decision date: 1989-07-25
Classification & Regulation
This clearance is catalogued under FDA product code GEH and 21 CFR 878.4350, within the General, Plastic Surgery review panel as a Class II device.