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ALLY PLATFORM SYSTEM

K093895 Class II Traditional
Decision Date
2010-05-20
Sponsor / Applicant
Continuity Health Solutions

Technical Specification

510(k) Submission ID K093895
Product Code DRG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2910
Decision Date 2010-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALLY PLATFORM SYSTEM received FDA 510(k) clearance under submission number K093895, sponsored by Continuity Health Solutions. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-05-20.

Classification & Regulation

This clearance is catalogued under FDA product code DRG and 21 CFR 870.2910, within the Cardiovascular review panel as a Class II device.