Clearance Summary
MATTIOLI PULSE TWO/THREE PLUS FAMILY received FDA 510(k) clearance under submission number K100053, sponsored by Mattioli Engineering Corp.. 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 2010-03-10.
- Submission: K100053
- Applicant / Sponsor: Mattioli Engineering Corp.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2010-03-10
Classification & Regulation
This clearance is catalogued under FDA product code ONF and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.