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PICCOLO PHOSPHORUS TEST SYSTEM

K022312 Class I Traditional
Decision Date
2002-09-05
Sponsor / Applicant
Abaxis, Inc.

Technical Specification

510(k) Submission ID K022312
Product Code CEO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1580
Decision Date 2002-09-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PICCOLO PHOSPHORUS TEST SYSTEM received FDA 510(k) clearance under submission number K022312, sponsored by Abaxis, Inc.. 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 2002-09-05.

Classification & Regulation

This clearance is catalogued under FDA product code CEO and 21 CFR 862.1580, within the Clinical Chemistry review panel as a Class I device.