Clearance Summary
CLP LIPOPROTEIN ELECTROPHORESIS CONTROL received FDA 510(k) clearance under submission number K881113, sponsored by Creative Laboratory Products, 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 1988-07-01.
- Submission: K881113
- Applicant / Sponsor: Creative Laboratory Products, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1660
- Decision date: 1988-07-01
Classification & Regulation
This clearance is catalogued under FDA product code JJY and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.