Ultrasonic Mesh Nebulizer

Nebulizer (direct Patient Interface)

Shenzhen Ivankaca Technology Co., Ltd

The following data is part of a premarket notification filed by Shenzhen Ivankaca Technology Co., Ltd with the FDA for Ultrasonic Mesh Nebulizer.

Pre-market Notification Details

Device IDK201397
510k NumberK201397
Device Name:Ultrasonic Mesh Nebulizer
ClassificationNebulizer (direct Patient Interface)
Applicant Shenzhen Ivankaca Technology Co., Ltd 3/F, Building B, No. 45 Lixin Road, NanWan, Longgang, Shenzhen, Guangdong Shenzhen,  CN 518100
ContactSam Wong
CorrespondentLong Yang
Shenzhen Hlongmed Biotech Co., Ltd. 1201, Haosheng Business Center, 4096 Dongbin Road, Nanshan, Shenzhen, P.R.C Shenzhen,  CN 518054
Product CodeCAF  
CFR Regulation Number868.5630 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2020-05-28
Decision Date2021-06-14

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
06971209160090 K201397 000
06971209160083 K201397 000

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