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CLIRANS BLOOD LINES SET

K771693 Class II Traditional
Decision Date
1977-09-20
Sponsor / Applicant
Terumo America, Inc.

Technical Specification

510(k) Submission ID K771693
Product Code FJK
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1977-09-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLIRANS BLOOD LINES SET received FDA 510(k) clearance under submission number K771693, sponsored by Terumo America, 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 1977-09-20.

Classification & Regulation

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