Clearance Summary
AMPLAID 770 ADMITTANCE METER received FDA 510(k) clearance under submission number K903066, sponsored by Amplus Corp.. 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 1990-10-24.
- Submission: K903066
- Applicant / Sponsor: Amplus Corp.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.1090
- Decision date: 1990-10-24
Classification & Regulation
This clearance is catalogued under FDA product code ETY and 21 CFR 874.1090, within the Ear, Nose, Throat review panel as a Class II device.