Clearance Summary
ULTRA LYTE ANALYZER I 100 received FDA 510(k) clearance under submission number K842315, sponsored by Ultra Quest Diagnostics, 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 1984-08-02.
- Submission: K842315
- Applicant / Sponsor: Ultra Quest Diagnostics, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1600
- Decision date: 1984-08-02
Classification & Regulation
This clearance is catalogued under FDA product code CEM and 21 CFR 862.1600, within the Clinical Chemistry review panel as a Class II device.