Angiplast Private , Ltd.

Angiplast Private , Ltd. holds 1 FDA 510(k) medical device clearance, cleared in 2002.

Top product codes for Angiplast Private , Ltd.

LHI — General Hospital1 device

Recent clearances by Angiplast Private , Ltd.

K012189 — ANGELTOUCH VENTED IV ADMINISTRATION SETCode LHI·2002-03-05

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