meddevicedb.com FDA Device Reference

LIPASE COLOR [TOYO] SERUM LIPASE TEST KIT

K897150 Class I Traditional
Decision Date
1990-02-26
Sponsor / Applicant
Toyo Jozo Co., Ltd.

Technical Specification

510(k) Submission ID K897150
Product Code CHI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1465
Decision Date 1990-02-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIPASE COLOR [TOYO] SERUM LIPASE TEST KIT received FDA 510(k) clearance under submission number K897150, sponsored by Toyo Jozo Co., Ltd.. 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 1990-02-26.

Classification & Regulation

This clearance is catalogued under FDA product code CHI and 21 CFR 862.1465, within the Clinical Chemistry review panel as a Class I device.