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STANBIO ALKALINE PHOSPHATASE (LIQUICOLOR) TEST SET

K941313 Class II Traditional
Decision Date
1994-05-17
Sponsor / Applicant
Stanbio Laboratory

Technical Specification

510(k) Submission ID K941313
Product Code CJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1050
Decision Date 1994-05-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STANBIO ALKALINE PHOSPHATASE (LIQUICOLOR) TEST SET received FDA 510(k) clearance under submission number K941313, sponsored by Stanbio Laboratory. 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 1994-05-17.

Classification & Regulation

This clearance is catalogued under FDA product code CJE and 21 CFR 862.1050, within the Clinical Chemistry review panel as a Class II device.