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SYSTEMATE(TM) ALKALINE PHOSPHATASE ITEM #65402

K895250 Class II Traditional
Decision Date
1989-10-31
Sponsor / Applicant
Em Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K895250
Product Code CJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1050
Decision Date 1989-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYSTEMATE(TM) ALKALINE PHOSPHATASE ITEM #65402 received FDA 510(k) clearance under submission number K895250, sponsored by Em Diagnostic 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 1989-10-31.

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.