510(k) K211572

Aesculap Slim Clip Applier by Aesculap, Inc. — Product Code HCI

K211572 is an FDA 510(k) premarket notification submitted by Aesculap, Inc. for the device "Aesculap Slim Clip Applier". The FDA issued a decision of Substantially Equivalent on December 13, 2021. The device falls under product code HCI (Applier, Aneurysm Clip), a Class II device regulated under 21 CFR 882.4175. Aesculap, Inc. has at least 10 other 510(k) clearances on record.