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MONITORING & STRESS TESTING EQUIPMENT

K760368 Class II Traditional
Decision Date
1977-02-28
Sponsor / Applicant
Advanced Medical, Inc.

Technical Specification

510(k) Submission ID K760368
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1977-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MONITORING & STRESS TESTING EQUIPMENT received FDA 510(k) clearance under submission number K760368, sponsored by Advanced 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 1977-02-28.

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.