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AMYLASE REAGENT

K912519 Class II Traditional
Decision Date
1991-07-01
Sponsor / Applicant
Genzyme Corp.

Technical Specification

510(k) Submission ID K912519
Product Code JFJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1070
Decision Date 1991-07-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AMYLASE REAGENT received FDA 510(k) clearance under submission number K912519, sponsored by Genzyme Corp.. 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 1991-07-01.

Classification & Regulation

This clearance is catalogued under FDA product code JFJ and 21 CFR 862.1070, within the Clinical Chemistry review panel as a Class II device.