510(k) K142252

XprESS Multi-Sinus Dilation Tool by Entellus Medical, Inc. — Product Code LRC

K142252 is an FDA 510(k) premarket notification submitted by Entellus Medical, Inc. for the device "XprESS Multi-Sinus Dilation Tool". The FDA issued a decision of Substantially Equivalent on October 17, 2014. The device falls under product code LRC (Instrument, Ent Manual Surgical), a Class I device regulated under 21 CFR 874.4420. Entellus Medical, Inc. has at least 10 other 510(k) clearances on record.