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FDA 510(k) Application Details - K182553
Device Classification Name
Wire, Guide, Catheter
More FDA Info for this Device
510(K) Number
K182553
Device Name
Wire, Guide, Catheter
Applicant
Suzhou Innomed Medical Device Co.,Ltd
218 Xinghu St., #B1-404
Suzhou 215123 CN
Other 510(k) Applications for this Company
Contact
Irene Ding
Other 510(k) Applications for this Contact
Regulation Number
870.1330
More FDA Info for this Regulation Number
Classification Product Code
DQX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/17/2018
Decision Date
03/11/2019
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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