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Shenzhen Kingyield Technology Co., Ltd

Shen Zhen Guangdong, CN

SHENZHEN KINGYIELD TECHNOLOGY CO., LTD appears in FDA device records in Shen Zhen Guangdong, CN. FDA records list 5 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
5
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 5 510(k) clearances for Shenzhen Kingyield Technology Co., Ltd between 2008 and 2018. The busiest year on record is 2008, with 1. The most recent is 2018, with 1.

Clearances by year, as a table
510(k) clearance decisions for Shenzhen Kingyield Technology Co., Ltd, by decision year
YearClearances
20081
20121
20131
20171
20181
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K182018Bluetooth blood pressure monitorDXNSubstantially Equivalent
K161530Bluetooth blood pressure monitorDXNSubstantially Equivalent
K123801FINGER PULSE OXIMETERDQASubstantially Equivalent
K112042KINGYIELD WRIST BLOOD PRESSURE MONITORDXNSubstantially Equivalent
K083043KING`YIELD WRIST BLOOD PRESSURE MONITOR, MODEL BP201DXNSubstantially Equivalent

Registered establishments

FDA registered establishments for Shenzhen Kingyield Technology Co., Ltd, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30074208563007420856SHENZHEN KINGYIELD TECHNOLOGY CO., LTDNo. 301, Bldg 1, Cuigang Industrail Zone 3, Huaide Community, Shen Zhen Guangdong 518103 CN2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain