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HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM

K872582 Class I Traditional
Decision Date
1987-07-16
Sponsor / Applicant
Millipore Corp.

Technical Specification

510(k) Submission ID K872582
Product Code LDM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2260
Decision Date 1987-07-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM received FDA 510(k) clearance under submission number K872582, sponsored by Millipore Corp.. 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 1987-07-16.

Classification & Regulation

This clearance is catalogued under FDA product code LDM and 21 CFR 862.2260, within the Clinical Chemistry review panel as a Class I device.