510(k) K222052

VitroPRO by CIVCO Medical Instruments Co., Inc. — Product Code ITX

K222052 is an FDA 510(k) premarket notification submitted by CIVCO Medical Instruments Co., Inc. for the device "VitroPRO". The FDA issued a decision of Substantially Equivalent on November 22, 2022. The device falls under product code ITX (Transducer, Ultrasonic, Diagnostic), a Class II device regulated under 21 CFR 892.1570. CIVCO Medical Instruments Co., Inc. has at least 10 other 510(k) clearances on record.