Clearance Summary
ANEMIAPRO SELF-SCREENER received FDA 510(k) clearance under submission number K042379, sponsored by Biosafe Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2004-12-15.
- Submission: K042379
- Applicant / Sponsor: Biosafe Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7500
- Decision date: 2004-12-15
Classification & Regulation
This clearance is catalogued under FDA product code KHG and 21 CFR 864.7500, within the Hematology review panel as a Class II device.