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AUTION CHECK PLUS

K142262 Class I Traditional
Decision Date
2015-04-10
Sponsor / Applicant
Quantimetrix Corp.

Technical Specification

510(k) Submission ID K142262
Product Code JJW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 2015-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTION CHECK PLUS received FDA 510(k) clearance under submission number K142262, sponsored by Quantimetrix Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2015-04-10.

Classification & Regulation

This clearance is catalogued under FDA product code JJW and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.