meddevicedb.com FDA Device Reference

ENZYMATIC AMYLASE REAGENT KIT

K760415 Class II Traditional
Decision Date
1976-11-05
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K760415
Product Code CIJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1070
Decision Date 1976-11-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENZYMATIC AMYLASE REAGENT KIT received FDA 510(k) clearance under submission number K760415, sponsored by Beckman Instruments, 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 1976-11-05.

Classification & Regulation

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