Clearance Summary
GLOOKO DEVICE SYSTEM FOR GLOOKO APPLICATION received FDA 510(k) clearance under submission number K132272, sponsored by Glooko, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2013-10-17.
- Submission: K132272
- Applicant / Sponsor: Glooko, Inc.
- Clearance pathway: Special
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1345
- Decision date: 2013-10-17
Classification & Regulation
This clearance is catalogued under FDA product code NBW and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.