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SPACELABS MEDICAL WORKSTATION

K860834 Class II Traditional
Decision Date
1986-04-29
Sponsor / Applicant
Spacelabs, Inc.

Technical Specification

510(k) Submission ID K860834
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1986-04-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPACELABS MEDICAL WORKSTATION received FDA 510(k) clearance under submission number K860834, sponsored by Spacelabs, 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 1986-04-29.

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.