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PARAGON ELECTROPHORESIS SYS LIPOPROTEIN REAGENT TE

K854057 Class I Traditional
Decision Date
1985-12-05
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K854057
Product Code JHO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1475
Decision Date 1985-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PARAGON ELECTROPHORESIS SYS LIPOPROTEIN REAGENT TE received FDA 510(k) clearance under submission number K854057, sponsored by Beckman 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 1985-12-05.

Classification & Regulation

This clearance is catalogued under FDA product code JHO and 21 CFR 862.1475, within the Clinical Chemistry review panel as a Class I device.