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EMDS GLUCOSE (GLU-HK) TEST, ITEM 65415

K924572 Class II Traditional
Decision Date
1992-11-25
Sponsor / Applicant
Em Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K924572
Product Code CFR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 1992-11-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMDS GLUCOSE (GLU-HK) TEST, ITEM 65415 received FDA 510(k) clearance under submission number K924572, 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 1992-11-25.

Classification & Regulation

This clearance is catalogued under FDA product code CFR and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.