Clearance Summary
ACUTEK'S CLEARPASAGE received FDA 510(k) clearance under submission number K962698, sponsored by Acutek Adhesive Specialties, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1996-09-09.
- Submission: K962698
- Applicant / Sponsor: Acutek Adhesive Specialties, Inc.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.3900
- Decision date: 1996-09-09
Classification & Regulation
This clearance is catalogued under FDA product code LWF and 21 CFR 874.3900, within the Ear, Nose, Throat review panel as a Class I device.