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FDA 510(k)

LIPASE LINEARITY CONTROL

K-Number: K913585 · 1991-10-21

ApplicantCreative Laboratory Products, Inc.
Decision Date1991-10-21
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIPASE LINEARITY CONTROL 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 1991-10-21 under 510(k) number K913585. 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 LIPASE LINEARITY CONTROL?

LIPASE LINEARITY CONTROL is a medical device that received FDA 510(k) clearance on 1991-10-21. The listed applicant is Creative Laboratory Products, Inc.. The 510(k) number is K913585.

When did LIPASE LINEARITY CONTROL receive FDA 510(k) clearance?

LIPASE LINEARITY CONTROL received FDA 510(k) clearance on 1991-10-21, under 510(k) number K913585.

Who is the listed applicant for LIPASE LINEARITY 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 LIPASE LINEARITY CONTROL?

The FDA product code for LIPASE LINEARITY CONTROL is JJX.

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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.

K950589CLP HIGH LEVEL HIGH DENSITY LIPO PROTEIN CHOLESTEROL CONTROL-HLK942284CLP TOTAL IRON AND UIBC/TIBC LINEARITY CONTROL SETK922995LIPID CONTROLSK913427SICKLE HEMOGLOBIN (HBA/S) CONTROL SETK913371TOTAL IRON AND UNSAT IRON BIND CAPAC/IRON BIND CALK913224LIPID LINEARITY CONTROLS

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Related Devices (Code: JJX)

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

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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