SUCTION PUMP

Apparatus, Suction, Ward Use, Portable, Ac-powered

DING HWA CO., LTD

The following data is part of a premarket notification filed by Ding Hwa Co., Ltd with the FDA for Suction Pump.

Pre-market Notification Details

Device IDK140031
510k NumberK140031
Device Name:SUCTION PUMP
ClassificationApparatus, Suction, Ward Use, Portable, Ac-powered
Applicant DING HWA CO., LTD 1083 DELAWARE AVE. Buffalo,  NY  14223
ContactRobert O Dean
CorrespondentRobert O Dean
DING HWA CO., LTD 1083 DELAWARE AVE. Buffalo,  NY  14223
Product CodeJCX  
CFR Regulation Number878.4780 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2014-01-06
Decision Date2014-04-28
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
14712946602554 K140031 000

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