Clearance Summary
MODEL 2740 CLINICAL REFRACTOMETER received FDA 510(k) clearance under submission number K941903, sponsored by Vee Gee Scientific, 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 1995-01-17.
- Submission: K941903
- Applicant / Sponsor: Vee Gee Scientific, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2800
- Decision date: 1995-01-17
Classification & Regulation
This clearance is catalogued under FDA product code JRE and 21 CFR 862.2800, within the Clinical Chemistry review panel as a Class I device.