Clearance Summary
HUMAPEN MEMOIR received FDA 510(k) clearance under submission number K053563, sponsored by Eli Lilly and Company. 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 2006-04-07.
- Submission: K053563
- Applicant / Sponsor: Eli Lilly and Company
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5860
- Decision date: 2006-04-07
Classification & Regulation
This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.