Clearance Summary
TUBE-BANDAGE FOR HUMAN DIGITS 200 received FDA 510(k) clearance under submission number K840107, sponsored by Zens Health Care Products. 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 1984-04-25.
- Submission: K840107
- Applicant / Sponsor: Zens Health Care Products
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.5075
- Decision date: 1984-04-25
Classification & Regulation
This clearance is catalogued under FDA product code FQM and 21 CFR 880.5075, within the General Hospital review panel as a Class I device.