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MICROSTAR VC1 VOLUMETRIC CYCLER

K832141 Class II Traditional
Decision Date
1983-10-14
Sponsor / Applicant
Medionics International , Ltd.

Technical Specification

510(k) Submission ID K832141
Product Code FKX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 1983-10-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROSTAR VC1 VOLUMETRIC CYCLER received FDA 510(k) clearance under submission number K832141, sponsored by Medionics International , Ltd.. 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 1983-10-14.

Classification & Regulation

This clearance is catalogued under FDA product code FKX and 21 CFR 876.5630, within the Gastroenterology, Urology review panel as a Class II device.