Clearance Summary
FIRST AID KIT received FDA 510(k) clearance under submission number K921976, sponsored by The Home Emergency Room. 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 1992-09-10.
- Submission: K921976
- Applicant / Sponsor: The Home Emergency Room
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 1992-09-10
Classification & Regulation
This clearance is catalogued under FDA product code LYY and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.