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MEDILOG DARWIN HOLTER ANALYSIS

K053369 Class II Traditional
Decision Date
2005-12-22
Sponsor / Applicant
Huntleigh Healthcare

Technical Specification

510(k) Submission ID K053369
Product Code DQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1425
Decision Date 2005-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDILOG DARWIN HOLTER ANALYSIS received FDA 510(k) clearance under submission number K053369, sponsored by Huntleigh Healthcare. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2005-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code DQK and 21 CFR 870.1425, within the Cardiovascular review panel as a Class II device.