CLP ELEVATED LIPID CONTROL
K-Number: K895858 · 1990-01-26
Advertisement
Device Summary
Frequently Asked Questions
What is the CLP ELEVATED LIPID CONTROL?
CLP ELEVATED LIPID CONTROL is a medical device that received FDA 510(k) clearance on 1990-01-26. The listed applicant is Creative Laboratory Products, Inc.. The 510(k) number is K895858.
When did CLP ELEVATED LIPID CONTROL receive FDA 510(k) clearance?
CLP ELEVATED LIPID CONTROL received FDA 510(k) clearance on 1990-01-26, under 510(k) number K895858.
Who is the listed applicant for CLP ELEVATED LIPID CONTROL?
The FDA 510(k) record lists Creative Laboratory Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLP ELEVATED LIPID CONTROL?
The FDA product code for CLP ELEVATED LIPID CONTROL is LYY.
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 Creative Laboratory Products, Inc. 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: LYY)
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