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URIC-ACID

K813511 Class I Traditional
Decision Date
1981-12-31
Sponsor / Applicant
Medical Analysis Systems, Inc.

Technical Specification

510(k) Submission ID K813511
Product Code KNK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1775
Decision Date 1981-12-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URIC-ACID received FDA 510(k) clearance under submission number K813511, sponsored by Medical Analysis Systems, 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 1981-12-31.

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.