Clearance Summary
BAND-AID(R) BRAND LIQUID BANDAGE received FDA 510(k) clearance under submission number K062602, sponsored by Johnson & Johnson Consumer Companies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2006-12-11.
- Submission: K062602
- Applicant / Sponsor: Johnson & Johnson Consumer Companies, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.5090
- Decision date: 2006-12-11
Classification & Regulation
This clearance is catalogued under FDA product code KMF and 21 CFR 880.5090, within the General Hospital review panel as a Class I device.