DIRECT HDL-CHOLESTROL LIQUID
K-Number: K982341 · 1998-07-30
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Device Summary
Frequently Asked Questions
What is the DIRECT HDL-CHOLESTROL LIQUID?
DIRECT HDL-CHOLESTROL LIQUID is a medical device that received FDA 510(k) clearance on 1998-07-30. The listed applicant is Randox Laboratories, Ltd.. The 510(k) number is K982341.
When did DIRECT HDL-CHOLESTROL LIQUID receive FDA 510(k) clearance?
DIRECT HDL-CHOLESTROL LIQUID received FDA 510(k) clearance on 1998-07-30, under 510(k) number K982341.
Who is the listed applicant for DIRECT HDL-CHOLESTROL LIQUID?
The FDA 510(k) record lists Randox Laboratories, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIRECT HDL-CHOLESTROL LIQUID?
The FDA product code for DIRECT HDL-CHOLESTROL LIQUID is LBS.
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 Randox Laboratories, Ltd. 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: LBS)
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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