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ISSYS DRUG FLOW MONITOR

K050783 Class II Traditional
Decision Date
2006-02-22
Sponsor / Applicant
Integrated Sensing Systems, Inc.

Technical Specification

510(k) Submission ID K050783
Product Code FLN
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2420
Decision Date 2006-02-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ISSYS DRUG FLOW MONITOR received FDA 510(k) clearance under submission number K050783, sponsored by Integrated Sensing Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2006-02-22.

Classification & Regulation

This clearance is catalogued under FDA product code FLN and 21 CFR 880.2420, within the General Hospital review panel as a Class II device.