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DURAZYME CHOLESTEROL

K840368 Class I Traditional
Decision Date
1984-03-30
Sponsor / Applicant
American Monitor Corp.

Technical Specification

510(k) Submission ID K840368
Product Code CHH
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1175
Decision Date 1984-03-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DURAZYME CHOLESTEROL received FDA 510(k) clearance under submission number K840368, sponsored by American Monitor 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 1984-03-30.

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.