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LIQUID CHROMATO. COLUMNS

K880724 Class I Traditional
Decision Date
1988-05-27
Sponsor / Applicant
Supelco, Inc.

Technical Specification

510(k) Submission ID K880724
Product Code DPM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2260
Decision Date 1988-05-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIQUID CHROMATO. COLUMNS received FDA 510(k) clearance under submission number K880724, sponsored by Supelco, 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 1988-05-27.

Classification & Regulation

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