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QUIKREAD CHEM. ANALYZER & CHOLES. FOR WHOLE BLOOD

K890027 Class I Traditional
Decision Date
1989-04-26
Sponsor / Applicant
Photec Diagnostics, Inc.

Technical Specification

510(k) Submission ID K890027
Product Code CHH
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1175
Decision Date 1989-04-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUIKREAD CHEM. ANALYZER & CHOLES. FOR WHOLE BLOOD received FDA 510(k) clearance under submission number K890027, sponsored by Photec Diagnostics, 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 1989-04-26.

Classification & Regulation

This clearance is catalogued under FDA product code CHH and 21 CFR 862.1175, within the Clinical Chemistry review panel as a Class I device.