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FDA 510(k) Application Details - K203803
Device Classification Name
Clamp, Vascular
More FDA Info for this Device
510(K) Number
K203803
Device Name
Clamp, Vascular
Applicant
VASOInnovations, Inc
1260 Huntington Drive
Suite 208
South Pasadena, CA 91030 US
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Contact
Rajendra Gurudas Sardesai
Other 510(k) Applications for this Contact
Regulation Number
870.4450
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Classification Product Code
DXC
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More FDA Info for this Product Code
Date Received
12/28/2020
Decision Date
01/26/2021
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
Y
Expedited Review
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