Clearance Summary
CURETTE SET, ANTRUM, COAKLEY received FDA 510(k) clearance under submission number K872609, sponsored by Military Engineering, 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 1987-07-15.
- Submission: K872609
- Applicant / Sponsor: Military Engineering, Inc.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.4420
- Decision date: 1987-07-15
Classification & Regulation
This clearance is catalogued under FDA product code KAP and 21 CFR 874.4420, within the Ear, Nose, Throat review panel as a Class I device.