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ACON ON CALL VIVID PAL BLOOD GLUCOSE MONITORING SYSTEM

K122110 Class II Special
Decision Date
2012-11-21
Sponsor / Applicant
ACON Laboratories, Inc.

Technical Specification

510(k) Submission ID K122110
Product Code CGA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2012-11-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACON ON CALL VIVID PAL BLOOD GLUCOSE MONITORING SYSTEM received FDA 510(k) clearance under submission number K122110, sponsored by ACON Laboratories, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2012-11-21.

Classification & Regulation

This clearance is catalogued under FDA product code CGA and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.