FDA 510(k) Application Details - K210627

Device Classification Name	Introducer, Catheter   More FDA Info for this Device
510(K) Number	K210627
Device Name	Introducer, Catheter
Applicant	Oscor Inc. 3816 DeSoto Boulevard Palm Harbor, FL 34683 US Other 510(k) Applications for this Company
Contact	Doug Myers Other 510(k) Applications for this Contact
Regulation Number	870.1340   More FDA Info for this Regulation Number
Classification Product Code	DYB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/02/2021
Decision Date	06/03/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review