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Barrington Ventures, Ltd: FDA-registered device maker in Barrington, IL, United States, 13 510(k) clearances

Name: Barrington Ventures, Ltd FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Barrington Ventures, Ltd is registered with the FDA (registration 3003622639) in Barrington, IL, United States. It lists 19 device types. The FDA files 13 510(k) clearances under its listings, the newest dated March 31, 2016. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3003622639
Address: 28W206 Commercial Ave, Barrington, IL, United States, 60010
Owner or operator: Barrington Ventures, LTD (10029782)
Roles: Repackager or relabeler
First device listed: June 11, 2013
Registered through: 2026
Brand names listed: BV Medical, Contec, KaWe, Sonoplus 3000-DS

Devices it lists

Device	Product code	Class	Role	Source
Airway, Oropharyngeal, Anesthesiology	CAE	1	Repackager or relabeler	accessdata.fda.gov
Blood Pressure Cuff	DXQ	2	Repackager or relabeler	accessdata.fda.gov
Continuous Measurement Thermometer	FLL	2	Repackager or relabeler	accessdata.fda.gov
Electrocardiograph	DPS	2	Repackager or relabeler	accessdata.fda.gov
Forceps, General & Plastic Surgery	GEN	1	Repackager or relabeler	accessdata.fda.gov
Light, Examination, Medical, Battery Powered	KYT	1	Repackager or relabeler	accessdata.fda.gov
Mask, Oxygen, Non-Rebreathing	KGB	1	Repackager or relabeler	accessdata.fda.gov
Nebulizer (Direct Patient Interface)	CAF	2	Repackager or relabeler	accessdata.fda.gov
Otoscope	ERA	1	Repackager or relabeler	accessdata.fda.gov
Oximeter	DQA	2	Repackager or relabeler	accessdata.fda.gov
Pad, Heating, Powered	IRT	2	Repackager or relabeler	accessdata.fda.gov
Percussor	GWZ	1	Repackager or relabeler	accessdata.fda.gov
Scale, Stand-On, Patient	FRI	1	Repackager or relabeler	accessdata.fda.gov
Scissors, General, Surgical	LRW	1	Repackager or relabeler	accessdata.fda.gov
Specula Accessories	FXG	1	Repackager or relabeler	accessdata.fda.gov
Stethoscope, Manual	LDE	1	Repackager or relabeler	accessdata.fda.gov
System, Measurement, Blood-Pressure, Non-Invasive	DXN	2	Repackager or relabeler	accessdata.fda.gov
Tape, Measuring, Rulers And Calipers	FTY	1	Repackager or relabeler	accessdata.fda.gov
Tourniquet, Nonpneumatic	GAX	1	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
March 31, 2016	K153146	Infrared Ear Thermometer	FLL	Substantially Equivalent	Sejoy Electronics & Instruments Co., Ltd.	accessdata.fda.gov
August 28, 2014	K140582	FINGERTIP PULSE OXIMETER	DQA	Substantially Equivalent	Shenzhen Jumper Medical Equipment Co., Ltd.	accessdata.fda.gov
August 24, 2011	K110776	DIGITAL THERMOMETER MT SERIES	FLL	Substantially Equivalent	Sejoy Electronics & Instruments Co., Ltd.	accessdata.fda.gov
May 13, 2011	K110774	ELECTRONIC SPHYGMOMANOMETER	DXN	Substantially Equivalent	Contec Medical System Co., Ltd.	accessdata.fda.gov
January 7, 2010	K092447	DIGITAL THERMOMETER (WITH DISPOSABLE THERMOMETER COVER), DT SERIES	FLL	Substantially Equivalent	Hangzhou Hua'An Medical & Health Instruments Co.,	accessdata.fda.gov
October 28, 2009	K092245	ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100	DXQ	Substantially Equivalent	Honsun (Nantong) Co., Ltd.	accessdata.fda.gov
September 17, 2008	K082542	ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE MODEL HBPK-A	DXQ	Substantially Equivalent	Cardicare Company, Ltd.	accessdata.fda.gov
July 13, 2007	K063641	PC-60, NON-INVASIVEPULSE OXIMETER	DQA	Substantially Equivalent	Shenzhen Creative Industry Co., Ltd.	accessdata.fda.gov
June 8, 2007	K062484	FLAEM NUOVA RF6 BASIC AND RF6 PLUS NEBULIZERS	CAF	Substantially Equivalent	Flaem Nuova S.P.A.	accessdata.fda.gov
February 6, 2006	K051699	SEJOY, MODEL MT-403	FLL	Substantially Equivalent	Sejoy Electronics & Instruments Co., Ltd.	accessdata.fda.gov
May 19, 2005	K051126	CARDIOSCOPE SONOPLUS 3000	DPS	Substantially Equivalent	Pulsonic Ag, Medical Technology	accessdata.fda.gov
August 16, 2001	K012444	ABN ANEROID SPHYGMOMANOMETER	DXQ	Substantially Equivalent	Pt. Sugih Instrumendo Abadi	accessdata.fda.gov
July 17, 1978	K780715	ANEROID TYPE BLOOD PRESSURE KIT	DXQ	Substantially Equivalent	Mars Metal Co., Ltd.	accessdata.fda.gov

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Updated March 31, 2016. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.