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DIALYSATE METER RS-2100A, CIRCUIT CHANGE

K770263 Class II Traditional
Decision Date
1977-02-18
Sponsor / Applicant
Renal Systems, Inc.

Technical Specification

510(k) Submission ID K770263
Product Code FLB
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1977-02-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIALYSATE METER RS-2100A, CIRCUIT CHANGE received FDA 510(k) clearance under submission number K770263, sponsored by Renal Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1977-02-18.

Classification & Regulation

This clearance is catalogued under FDA product code FLB and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.