FDA 510(k)

LIPID CONTROLS

K-Number: K922995 · 1992-08-12

ApplicantCreative Laboratory Products, Inc.

Decision Date1992-08-12

Product CodeJJX

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

LIPID CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Creative Laboratory Products, Inc.. It received FDA 510(k) clearance on 1992-08-12 under 510(k) number K922995. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIPID CONTROLS?

LIPID CONTROLS is a medical device that received FDA 510(k) clearance on 1992-08-12. The listed applicant is Creative Laboratory Products, Inc.. The 510(k) number is K922995.

When did LIPID CONTROLS receive FDA 510(k) clearance?

LIPID CONTROLS received FDA 510(k) clearance on 1992-08-12, under 510(k) number K922995.

Who is the listed applicant for LIPID CONTROLS?

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 LIPID CONTROLS?

The FDA product code for LIPID CONTROLS is JJX.

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Other records listing Creative Laboratory Products, Inc. as applicant

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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.