Embol-X, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Embol-X, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Embol-X, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 4 cleared submissions from 1999 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Embol-X, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Embol-X, Inc.
4 devices
Cleared
Feb 14, 2003
EMBOL-X AORTIC FILTERS,ETRA-SMALL,SMALL,MEDIUM,LARGE,EXTRA LARGE,MODELS...
Cardiovascular
233d
Cleared
Sep 05, 2002
AORTIC CANNULA, METAL J-TIP (24FR) MODEL #CF00100
Cardiovascular
185d
Cleared
Apr 26, 2001
EMBOL-X INTRODUCER, MODEL CF00200
Cardiovascular
216d
Cleared
Feb 02, 1999
EMBOL-X AORTIC OCCLUSION AND CARDIOPLEGIA CANNULA
Cardiovascular
349d