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FDA 510(k)

LIQUISPX LIQUID LIPID CONTROL

K-Number: K012855 · 2001-08-30

ApplicantClinical Controls Division
Decision Date2001-08-30
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUISPX LIQUID LIPID CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Controls Division. It received FDA 510(k) clearance on 2001-08-30 under 510(k) number K012855. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUISPX LIQUID LIPID CONTROL?

LIQUISPX LIQUID LIPID CONTROL is a medical device that received FDA 510(k) clearance on 2001-08-30. The listed applicant is Clinical Controls Division. The 510(k) number is K012855.

When did LIQUISPX LIQUID LIPID CONTROL receive FDA 510(k) clearance?

LIQUISPX LIQUID LIPID CONTROL received FDA 510(k) clearance on 2001-08-30, under 510(k) number K012855.

Who is the listed applicant for LIQUISPX LIQUID LIPID CONTROL?

The FDA 510(k) record lists Clinical Controls Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIQUISPX LIQUID LIPID CONTROL?

The FDA product code for LIQUISPX LIQUID LIPID CONTROL is JJY.

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Related Devices (Code: JJY)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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