Clearance Summary
LKB 2160 MIDISPIN CENTRIFUGE received FDA 510(k) clearance under submission number K831947, sponsored by Lkb Instruments, 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 1983-07-29.
- Submission: K831947
- Applicant / Sponsor: Lkb Instruments, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2050
- Decision date: 1983-07-29
Classification & Regulation
This clearance is catalogued under FDA product code JQC and 21 CFR 862.2050, within the Clinical Chemistry review panel as a Class I device.