Clearance Summary
AUTOMATED GYLCOHEMOGLOBIN ANALYZER HLC-723G8 received FDA 510(k) clearance under submission number K131580, sponsored by Tosoh Bioscience, Inc.. 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 2014-01-23.
- Submission: K131580
- Applicant / Sponsor: Tosoh Bioscience, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1373
- Decision date: 2014-01-23
Classification & Regulation
This clearance is catalogued under FDA product code PDJ and 21 CFR 862.1373, within the Clinical Chemistry review panel as a Class II device.