Angioslide, Ltd.

6 FDA 510(k) medical device clearances.

Top product codes for Angioslide, Ltd.

LIT — Cardiovascular 5 devices
DQY — Cardiovascular 1 device

Recent clearances by Angioslide, Ltd.

K172494 — PROTEUS PTA Balloon Catheter with Embolic Capture Feature LIT · 2017-12-15
K133043 — PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE LIT · 2013-12-06
K120164 — PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE LIT · 2012-06-08
K120805 — PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE LIT · 2012-04-13
K111750 — EXTRA PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE; PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE DQY · 2011-07-21
K090364 — EXTRA PTA BALLOON CATHETER WITH EMBOLIC PROTECTION FEATURE LIT · 2010-03-23

Data sourced from openFDA. This site is unofficial and independent of the FDA.