Clearance Summary
EYE PAD received FDA 510(k) clearance under submission number K904896, sponsored by Ulti-Med Intl., 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 1990-12-05.
- Submission: K904896
- Applicant / Sponsor: Ulti-Med Intl., Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4440
- Decision date: 1990-12-05
Classification & Regulation
This clearance is catalogued under FDA product code HMP and 21 CFR 878.4440, within the General, Plastic Surgery review panel as a Class I device.