Clearance Summary
TEARLAB OSMOLARITY SYSTEM received FDA 510(k) clearance under submission number K083184, sponsored by Ocusense, 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 2009-05-14.
- Submission: K083184
- Applicant / Sponsor: Ocusense, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1540
- Decision date: 2009-05-14
Classification & Regulation
This clearance is catalogued under FDA product code OND and 21 CFR 862.1540, within the Clinical Chemistry review panel as a Class I device.