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ULTRAFILTRATION SCALE

K781633 Class II Traditional
Decision Date
1978-12-07
Sponsor / Applicant
Extracorporeal Medical Specialities, Inc.

Technical Specification

510(k) Submission ID K781633
Product Code FIL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1978-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRAFILTRATION SCALE received FDA 510(k) clearance under submission number K781633, sponsored by Extracorporeal Medical Specialities, 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 1978-12-07.

Classification & Regulation

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