HDL-CHOLESTEROL PLUS 2ND GENERATION
K-Number: K033610 · 2003-12-05
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Device Summary
Frequently Asked Questions
What is the HDL-CHOLESTEROL PLUS 2ND GENERATION?
HDL-CHOLESTEROL PLUS 2ND GENERATION is a medical device that received FDA 510(k) clearance on 2003-12-05. The listed applicant is Roche Diagnostics Corp.. The 510(k) number is K033610.
When did HDL-CHOLESTEROL PLUS 2ND GENERATION receive FDA 510(k) clearance?
HDL-CHOLESTEROL PLUS 2ND GENERATION received FDA 510(k) clearance on 2003-12-05, under 510(k) number K033610.
Who is the listed applicant for HDL-CHOLESTEROL PLUS 2ND GENERATION?
The FDA 510(k) record lists Roche Diagnostics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HDL-CHOLESTEROL PLUS 2ND GENERATION?
The FDA product code for HDL-CHOLESTEROL PLUS 2ND GENERATION 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 Roche Diagnostics 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: 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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