Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LIPID LINEARITY CONTROLS

K-Number: K913224 · 1991-09-25

ApplicantCreative Laboratory Products, Inc.
Decision Date1991-09-25
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIPID LINEARITY 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 1991-09-25 under 510(k) number K913224. 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 LIPID LINEARITY CONTROLS?

LIPID LINEARITY CONTROLS is a medical device that received FDA 510(k) clearance on 1991-09-25. The listed applicant is Creative Laboratory Products, Inc.. The 510(k) number is K913224.

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

LIPID LINEARITY CONTROLS received FDA 510(k) clearance on 1991-09-25, under 510(k) number K913224.

Who is the listed applicant for LIPID LINEARITY 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 LINEARITY CONTROLS?

The FDA product code for LIPID LINEARITY CONTROLS is JJY.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

View all 27 devices →

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.

↑