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Shenzhen RF Tech Co., Ltd.

Shenzhen Guangdong, CN

Shenzhen RF Tech Co., Ltd. appears in FDA device records in Shenzhen Guangdong, CN. FDA records list 12 510(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
12
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 12 510(k) clearances for Shenzhen RF Tech Co., Ltd. between 2015 and 2026. The busiest year on record is 2023, with 3. The most recent is 2026, with 3.

Clearances by year, as a table
510(k) clearance decisions for Shenzhen RF Tech Co., Ltd., by decision year
YearClearances
20151
20162
20171
20201
20221
20233
20263
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K252587HD 8Ch Wrist ArrayMOSSubstantially Equivalent
K252876GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive Only; GEM Flex Coil 16-S Array, 3.0T Receive OnlyMOSSubstantially Equivalent
K252179GEM Flex Coil 16-L Array, 1.5T Receive Only; GEM Flex Coil 16-M Array, 1.5T Receive Only; GEM Flex Coil 16-S Array, 1.5T Receive OnlyMOSSubstantially Equivalent
K2310851.5T HD T/R Knee Array (10-F34127)MOSSubstantially Equivalent
K2232031.5T 24E Posterior ArrayLNHSubstantially Equivalent
K2232258ch T/R Knee CoilMOSSubstantially Equivalent
K2232398ch Wrist CoilMOSSubstantially Equivalent
K2008368ch Flex SuiteMOSSubstantially Equivalent
K1722228ch Flex SuiteMOSSubstantially Equivalent
K1609328ch Foot Ankle CoilMOSSubstantially Equivalent
K1609358ch Foot Ankle CoilMOSSubstantially Equivalent
K1516538ch Foot Ankle CoilMOSSubstantially Equivalent

Registered establishments

FDA registered establishments for Shenzhen RF Tech Co., Ltd., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30097552503009755250Shenzhen RF Tech Co., Ltd.601,602 of BLD1, Guangming Digital Intelligent Manufacturing Industrial Park,18th Xialang Road, Shenzhen Guangdong 518106 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