B&J DVT Compression Devices MHH800/MHH800SQ

Sleeve, Limb, Compressible

B & J Manufacturing Ltd.

The following data is part of a premarket notification filed by B & J Manufacturing Ltd. with the FDA for B&j Dvt Compression Devices Mhh800/mhh800sq.

Pre-market Notification Details

Device IDK200154
510k NumberK200154
Device Name:B&J DVT Compression Devices MHH800/MHH800SQ
ClassificationSleeve, Limb, Compressible
Applicant B & J Manufacturing Ltd. Room 701 & 101, Building 24, Block B, Yuanshan Industrial Zone, Gongming Shenzhen,  CN 518106
ContactBilly Yu
CorrespondentFu Ailing
Shenzhen Joyantech Consulting Co., Ltd. Room 1713A, 17F, Block A, Time Square, Xili Town Shenzhen,  CN 518055
Product CodeJOW  
CFR Regulation Number870.5800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2020-01-22
Decision Date2020-07-08

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