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Little Doctor Electronic(nantong) Co.,ltd: FDA-registered device maker in Nantong Jiangsu, China, 4 510(k) clearances

Name: Little Doctor Electronic(nantong) Co.,ltd FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Little Doctor Electronic(nantong) Co.,ltd is registered with the FDA (registration 3017303999) in Nantong Jiangsu, China. It lists 17 device types. The FDA files 4 510(k) clearances under its listings, the newest dated July 2, 2020. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3017303999
Address: No.14, Zhenxingxilu Road,Chongchuan Area, Nantong Jiangsu, China, 226000
Owner or operator: Little Doctor Electronic(Nantong) Co.,Ltd (10076383)
Roles: Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler, Specification developer
First device listed: July 16, 2020
Registered through: 2026
Brand names listed: Blood pressure kit, Blood pressure monitor, Compressor Nebulizer, FriCARE, Mirror, Nebulizer kit, PUMP, NEBULIZER, ELECTRICALLY POWERED, RECORDER, PAPER CHART and more

Devices it lists

Device	Product code	Class	Role	Source
Blood Pressure Cuff	DXQ	2	Manufacturer	accessdata.fda.gov
Compressor, Air, Portable	BTI	2	Manufacturer	accessdata.fda.gov
Depressor, Metal Tongue, Surgical	KBL	1	Specification developer	accessdata.fda.gov
Hammer, Surgical	FZY	1	Specification developer	accessdata.fda.gov
Light, Examination, Medical, Battery Powered	KYT	1	Specification developer	accessdata.fda.gov
Mirror, Ent	KAI	1	Specification developer	accessdata.fda.gov
Nebulizer (Direct Patient Interface)	CAF	2	Repackager or relabeler	accessdata.fda.gov
Ophthalmoscope, Battery-Powered	HLJ	2	Specification developer	accessdata.fda.gov
Otoscope	ERA	1	Specification developer	accessdata.fda.gov
Pump, Nebulizer, Electrically Powered	JPW	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Recorder, Paper Chart	DSF	1	Exporter to the US	accessdata.fda.gov
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	HOY	1	Exporter to the US	accessdata.fda.gov
Speculum, Ent	EPY	1	Specification developer	accessdata.fda.gov
Stethoscope, Manual	LDE	1	Manufacturer, Specification developer	accessdata.fda.gov
System, Measurement, Blood-Pressure, Non-Invasive	DXN	2	Manufacturer	accessdata.fda.gov
Tape, Measuring, Rulers And Calipers	FTY	1	Specification developer	accessdata.fda.gov
Tourniquet, Nonpneumatic	GAX	1	Specification developer	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
July 2, 2020	K193259	Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer	DXQ	Substantially Equivalent	Little Doctor Electronic (Nantong)Co.,Ltd	accessdata.fda.gov
May 15, 2013	K123800	WRIST AUTOMATIC BLOOD PRESSURE MONITOR	DXN	Substantially Equivalent	Little Doctor Electronic (Nantong)Co.,Ltd	accessdata.fda.gov
May 3, 2013	K123600	DIGITAL BLOOD PRESSURE MONITOR	DXN	Substantially Equivalent	Little Doctor Electronic (Nantong)Co.,Ltd	accessdata.fda.gov
November 10, 2009	K091272	BESMED JET NEBULIZER BOTTLE SET	CAF	Substantially Equivalent	Besmed Health Business Corp	accessdata.fda.gov

Compare with other makers

Updated July 2, 2020. 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.