CHOLESTECH LIPID MONITORING SYS.
K-Number: K912136 · 1991-07-30
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Device Summary
Frequently Asked Questions
What is the CHOLESTECH LIPID MONITORING SYS.?
CHOLESTECH LIPID MONITORING SYS. is a medical device that received FDA 510(k) clearance on 1991-07-30. The listed applicant is Cholestech Corp.. The 510(k) number is K912136.
When did CHOLESTECH LIPID MONITORING SYS. receive FDA 510(k) clearance?
CHOLESTECH LIPID MONITORING SYS. received FDA 510(k) clearance on 1991-07-30, under 510(k) number K912136.
Who is the listed applicant for CHOLESTECH LIPID MONITORING SYS.?
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 CHOLESTECH LIPID MONITORING SYS.?
The FDA product code for CHOLESTECH LIPID MONITORING SYS. 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.
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