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MODEL IDS640 PATIENT DATA DISPLAY & STORAGE MONIT.

K882352 Class II Traditional
Decision Date
1988-11-02
Sponsor / Applicant
Clinical Information Systems, Inc.

Technical Specification

510(k) Submission ID K882352
Product Code CCL
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.1720
Decision Date 1988-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL IDS640 PATIENT DATA DISPLAY & STORAGE MONIT. received FDA 510(k) clearance under submission number K882352, sponsored by Clinical Information Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1988-11-02.

Classification & Regulation

This clearance is catalogued under FDA product code CCL and 21 CFR 868.1720, within the Anesthesiology review panel as a Class II device.