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SPACELABS MEDICAL INTEGRATED MULTIPARAMETER MODULE 90496

K972502 Class II Traditional
Decision Date
1998-05-28
Sponsor / Applicant
Spacelabs Medical, Inc.

Technical Specification

510(k) Submission ID K972502
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1998-05-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPACELABS MEDICAL INTEGRATED MULTIPARAMETER MODULE 90496 received FDA 510(k) clearance under submission number K972502, sponsored by Spacelabs Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1998-05-28.

Classification & Regulation

This clearance is catalogued under FDA product code DSI and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.