Clearance Summary
AVENT NIPPLE SHIELD received FDA 510(k) clearance under submission number K944117, sponsored by Avent America, 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 1994-10-05.
- Submission: K944117
- Applicant / Sponsor: Avent America, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.5630
- Decision date: 1994-10-05
Classification & Regulation
This clearance is catalogued under FDA product code HFS and 21 CFR 880.5630, within the General Hospital review panel as a Class I device.