Clearance Summary
TYMPASNOSTOMY TUBE received FDA 510(k) clearance under submission number K953993, sponsored by Hampton Precision Products, 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 1995-09-12.
- Submission: K953993
- Applicant / Sponsor: Hampton Precision Products, Inc.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.3880
- Decision date: 1995-09-12
Classification & Regulation
This clearance is catalogued under FDA product code ETD and 21 CFR 874.3880, within the Ear, Nose, Throat review panel as a Class II device.