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GGT PROCEDURE OR GAMMA GLUTAMYL TRANSFERASE PROCED

K844720 Class I Traditional
Decision Date
1984-12-12
Sponsor / Applicant
Data Medical Associates, Inc.

Technical Specification

510(k) Submission ID K844720
Product Code JQB
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1360
Decision Date 1984-12-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GGT PROCEDURE OR GAMMA GLUTAMYL TRANSFERASE PROCED received FDA 510(k) clearance under submission number K844720, sponsored by Data Medical Associates, 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 1984-12-12.

Classification & Regulation

This clearance is catalogued under FDA product code JQB and 21 CFR 862.1360, within the Clinical Chemistry review panel as a Class I device.