Clearance Summary
LIPASE DETERMINATION received FDA 510(k) clearance under submission number K800550, sponsored by The Dow Chemical Co.. 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 1980-04-02.
- Submission: K800550
- Applicant / Sponsor: The Dow Chemical Co.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1465
- Decision date: 1980-04-02
Classification & Regulation
This clearance is catalogued under FDA product code CFG and 21 CFR 862.1465, within the Clinical Chemistry review panel as a Class I device.