Clearance Summary
DERMIVIEW CLEAR TAPE received FDA 510(k) clearance under submission number K942383, sponsored by Johnson & Johnson International. 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 1994-08-22.
- Submission: K942383
- Applicant / Sponsor: Johnson & Johnson International
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.5240
- Decision date: 1994-08-22
Classification & Regulation
This clearance is catalogued under FDA product code KGX and 21 CFR 880.5240, within the General Hospital review panel as a Class I device.