Clearance Summary
SKINTACT received FDA 510(k) clearance under submission number K024264, sponsored by Leonhard Lang Co.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-01-16.
- Submission: K024264
- Applicant / Sponsor: Leonhard Lang Co.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2360
- Decision date: 2003-01-16
Classification & Regulation
This clearance is catalogued under FDA product code DRX and 21 CFR 870.2360, within the Cardiovascular review panel as a Class II device.