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RIALYZE HPL (RIA)

K770659 Class II Traditional
Decision Date
1977-05-20
Sponsor / Applicant
Miles Laboratories, Inc.

Technical Specification

510(k) Submission ID K770659
Product Code JMF
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1585
Decision Date 1977-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RIALYZE HPL (RIA) received FDA 510(k) clearance under submission number K770659, sponsored by Miles Laboratories, 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 1977-05-20.

Classification & Regulation

This clearance is catalogued under FDA product code JMF and 21 CFR 862.1585, within the Clinical Chemistry review panel as a Class II device.