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URIC ACID, MODEL UA112-01

K991247 Class I Traditional
Decision Date
1999-05-25
Sponsor / Applicant
A.P. Total Care, Inc.

Technical Specification

510(k) Submission ID K991247
Product Code KNK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1775
Decision Date 1999-05-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URIC ACID, MODEL UA112-01 received FDA 510(k) clearance under submission number K991247, sponsored by A.P. Total Care, 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 1999-05-25.

Classification & Regulation

This clearance is catalogued under FDA product code KNK and 21 CFR 862.1775, within the Clinical Chemistry review panel as a Class I device.