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FDA 510(k)

CLP COMPREHENSIVE LIPID CONTROL-HR

K-Number: K896247 · 1990-01-10

ApplicantCreative Laboratory Products, Inc.
Decision Date1990-01-10
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CLP COMPREHENSIVE LIPID CONTROL-HR 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 1990-01-10 under 510(k) number K896247. 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 CLP COMPREHENSIVE LIPID CONTROL-HR?

CLP COMPREHENSIVE LIPID CONTROL-HR is a medical device that received FDA 510(k) clearance on 1990-01-10. The listed applicant is Creative Laboratory Products, Inc.. The 510(k) number is K896247.

When did CLP COMPREHENSIVE LIPID CONTROL-HR receive FDA 510(k) clearance?

CLP COMPREHENSIVE LIPID CONTROL-HR received FDA 510(k) clearance on 1990-01-10, under 510(k) number K896247.

Who is the listed applicant for CLP COMPREHENSIVE LIPID CONTROL-HR?

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 COMPREHENSIVE LIPID CONTROL-HR?

The FDA product code for CLP COMPREHENSIVE LIPID CONTROL-HR is JJY.

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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 CALK913585LIPASE LINEARITY CONTROL

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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.

K162530Multichem IA PlusTechno-Path ManufacturingK163629Audit MicroControls Linearity FD Tumor Markers IIAalto Scientific, Ltd.K163015Liquichek Tumor Marker Control-Level 1; Liquichek Tumor Marker Control-Level 2; Liquichek Tumor Marker Control-Level 3; Liquichek Tumor Marker Control- Trilevel MiniPakBio-Rad LaboratoriesK153712VK-3 Verification Kit, VK-4 Verification Kit, VK-R5 Verification Kit, VK-R7 Verification Kit, VK-Crea Verification KitRadiometer America, Inc.K132227LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-TRILEVEL, LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-LEVEL I, LIQUICHEK IMMUNOASSAYBio-Rad LaboratoriesK132156RANDOX CSF CONTROLS LEVELS 2 AND 3Randox Laboratories, Ltd.

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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