Clearance Summary
KAGER TRAPDUST received FDA 510(k) clearance under submission number K790085, sponsored by Kager Intl.. 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 1979-05-29.
- Submission: K790085
- Applicant / Sponsor: Kager Intl.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class:
- Decision date: 1979-05-29
Classification & Regulation
This clearance is catalogued under FDA product code LDQ , within the General Hospital review panel as a device.