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MICRO-COMPUTER ARRHYTHONIA SYSTEM

K760884 Class II Traditional
Decision Date
1976-12-09
Sponsor / Applicant
Spacelabs, Inc.

Technical Specification

510(k) Submission ID K760884
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1976-12-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRO-COMPUTER ARRHYTHONIA SYSTEM received FDA 510(k) clearance under submission number K760884, 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 1976-12-09.

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.