L.D.X LIPID MONITORING SYSTEM— 510(k) K901900

Substantially Equivalent

Cholestech Corp.

FDA 510(k) clearance K901900 for L.D.X LIPID MONITORING SYSTEM, Substantially Equivalent on 1990-07-24. Applicant: Cholestech Corp.. Device class: 1.

Clearance details

Applicant: Cholestech Corp.
Product code: Code CHH
Device class: Class 1
Regulation: 21 CFR 862.1175
Advisory panel: Clinical Chemistry
Date received: 1990-04-27
Decision date: 1990-07-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hayward, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.