L.D.X LIPID MONITORING SYSTEM
K-Number: K901900 · 1990-07-24
Advertisement
Device Summary
Frequently Asked Questions
What is the L.D.X LIPID MONITORING SYSTEM?
L.D.X LIPID MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1990-07-24. The listed applicant is Cholestech Corp.. The 510(k) number is K901900.
When did L.D.X LIPID MONITORING SYSTEM receive FDA 510(k) clearance?
L.D.X LIPID MONITORING SYSTEM received FDA 510(k) clearance on 1990-07-24, under 510(k) number K901900.
Who is the listed applicant for L.D.X LIPID MONITORING SYSTEM?
The FDA 510(k) record lists Cholestech Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for L.D.X LIPID MONITORING SYSTEM?
The FDA product code for L.D.X LIPID MONITORING SYSTEM is CHH.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Cholestech Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: CHH)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement