Clearance Summary
SKYTRON SKYBOOM SERIES received FDA 510(k) clearance under submission number K950192, sponsored by Skytron, Div. the Kmw Group, Inc.. 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 1995-04-03.
- Submission: K950192
- Applicant / Sponsor: Skytron, Div. the Kmw Group, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4960
- Decision date: 1995-04-03
Classification & Regulation
This clearance is catalogued under FDA product code FQO and 21 CFR 878.4960, within the General, Plastic Surgery review panel as a Class I device.