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FDA 510(k) Application Details - K213739
Device Classification Name
Polymer Patient Examination Glove
More FDA Info for this Device
510(K) Number
K213739
Device Name
Polymer Patient Examination Glove
Applicant
Hangzhou Runheng Medical Co., Ltd.
Room 201, Shunfeng Building, NO.109 Hongxing Road,
Qiaonan Block
Hangzhou 311215 CN
Other 510(k) Applications for this Company
Contact
Yaya Lu
Other 510(k) Applications for this Contact
Regulation Number
880.6250
More FDA Info for this Regulation Number
Classification Product Code
LZA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/29/2021
Decision Date
06/22/2022
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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