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DISPOSABLE ECG MONITORING ELECTRODES, MODELS 4060, 4610

K990112 Class II Traditional
Decision Date
1999-12-06
Sponsor / Applicant
Maersk Medical A/S

Technical Specification

510(k) Submission ID K990112
Product Code DRX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2360
Decision Date 1999-12-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE ECG MONITORING ELECTRODES, MODELS 4060, 4610 received FDA 510(k) clearance under submission number K990112, sponsored by Maersk Medical A/S. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1999-12-06.

Classification & Regulation

This clearance is catalogued under FDA product code DRX and 21 CFR 870.2360, within the Cardiovascular review panel as a Class II device.