Medical Device Manufacturer · US , Sandy Spring , MD

Angioslide, Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2010
6
Total
6
Cleared
0
Denied

Angioslide, Ltd. has 6 FDA 510(k) cleared medical devices. Based in Sandy Spring, US.

Historical record: 6 cleared submissions from 2010 to 2017. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Angioslide, Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Angioslide, Ltd.

6 devices
1-6 of 6
Cleared Dec 15, 2017
PROTEUS PTA Balloon Catheter with Embolic Capture Feature
K172494 · LIT
Cardiovascular · 119d
Cleared Dec 06, 2013
PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE
K133043 · LIT
Cardiovascular · 71d
Cleared Jun 08, 2012
PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE
K120164 · LIT
Cardiovascular · 141d
Cleared Apr 13, 2012
PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE
K120805 · LIT
Cardiovascular · 28d
Cleared Jul 21, 2011
EXTRA PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE
K111750 · DQY
Cardiovascular · 29d
Cleared Mar 23, 2010
EXTRA PTA BALLOON CATHETER WITH EMBOLIC PROTECTION FEATURE
K090364 · LIT
Cardiovascular · 403d
Filters
Filter by Specialty
All6 Cardiovascular 6