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SINGLE LEAD DIGITAL TELEMETRY TRANSMITTER

K952885 Class II Traditional
Decision Date
1995-09-26
Sponsor / Applicant
Spacelabs Medical, Inc.

Technical Specification

510(k) Submission ID K952885
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1995-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SINGLE LEAD DIGITAL TELEMETRY TRANSMITTER received FDA 510(k) clearance under submission number K952885, 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 1995-09-26.

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.