Clearance Summary
GEM PREMIER 3000 received FDA 510(k) clearance under submission number K052121, sponsored by Instrumentation Laboratory CO. 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 2005-10-21.
- Submission: K052121
- Applicant / Sponsor: Instrumentation Laboratory CO
- Clearance pathway: Special
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1345
- Decision date: 2005-10-21
Classification & Regulation
This clearance is catalogued under FDA product code CGA and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.