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DEOXYPYRIDINOLINE ASSAY FOR THE BAYER IMMUNO 1 SYSTEM

K972580 Class I Traditional
Decision Date
1997-09-22
Sponsor / Applicant
Bayer Corp.

Technical Specification

510(k) Submission ID K972580
Product Code JMM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1400
Decision Date 1997-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DEOXYPYRIDINOLINE ASSAY FOR THE BAYER IMMUNO 1 SYSTEM received FDA 510(k) clearance under submission number K972580, sponsored by Bayer 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 1997-09-22.

Classification & Regulation

This clearance is catalogued under FDA product code JMM and 21 CFR 862.1400, within the Clinical Chemistry review panel as a Class I device.