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GAMMA GLUTAMYL TRANSPEPTIDASE (GGTP) REAGENT SET

K860348 Class I Traditional
Decision Date
1986-03-17
Sponsor / Applicant
Sterling Diagnostics, Inc.

Technical Specification

510(k) Submission ID K860348
Product Code JPZ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1360
Decision Date 1986-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GAMMA GLUTAMYL TRANSPEPTIDASE (GGTP) REAGENT SET received FDA 510(k) clearance under submission number K860348, sponsored by Sterling Diagnostics, 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 1986-03-17.

Classification & Regulation

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