meddevicedb.com FDA Device Reference

OLYMPUS AMYLASE REAGENT

K944229 Class II Traditional
Decision Date
1994-12-09
Sponsor / Applicant
Olympus America, Inc.

Technical Specification

510(k) Submission ID K944229
Product Code JFJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1070
Decision Date 1994-12-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OLYMPUS AMYLASE REAGENT received FDA 510(k) clearance under submission number K944229, sponsored by Olympus America, 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 1994-12-09.

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.