Clearance Summary
EG V1 (BL) SELF MONITORING GLUCOSE TEST SYSTEM MODEL: EPS10017 received FDA 510(k) clearance under submission number K101037, sponsored by Eps Bio Technology Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2011-05-23.
- Submission: K101037
- Applicant / Sponsor: Eps Bio Technology Corp.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1345
- Decision date: 2011-05-23
Classification & Regulation
This clearance is catalogued under FDA product code LFR and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.