Clearance Summary
MERIVAARA CRIB TROLLEY-MODEL 381 received FDA 510(k) clearance under submission number K852173, sponsored by Daun International, Inc.. 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 1985-06-17.
- Submission: K852173
- Applicant / Sponsor: Daun International, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5140
- Decision date: 1985-06-17
Classification & Regulation
This clearance is catalogued under FDA product code FMS and 21 CFR 880.5140, within the General Hospital review panel as a Class II device.