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CRITERION II PACING SYSTEM MONITORS

K800286 Class II Traditional
Decision Date
1980-03-12
Sponsor / Applicant
Dart Medical Equipment

Technical Specification

510(k) Submission ID K800286
Product Code DTC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3630
Decision Date 1980-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CRITERION II PACING SYSTEM MONITORS received FDA 510(k) clearance under submission number K800286, sponsored by Dart Medical Equipment. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1980-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code DTC and 21 CFR 870.3630, within the Cardiovascular review panel as a Class II device.