510(k) K220006

angioLOCK Polymer Ligating Clip by A2 Medical Systems, LLC — Product Code FZP

K220006 is an FDA 510(k) premarket notification submitted by A2 Medical Systems, LLC for the device "angioLOCK Polymer Ligating Clip". The FDA issued a decision of Substantially Equivalent on March 2, 2022. The device falls under product code FZP (Clip, Implantable), a Class II device regulated under 21 CFR 878.4300. A2 Medical Systems, LLC has at least 1 other 510(k) clearance on record.