510(k) K181966

SmartPerfusion by Philips Medical Systems Nederlands B.V. — Product Code OWB

K181966 is an FDA 510(k) premarket notification submitted by Philips Medical Systems Nederlands B.V. for the device "SmartPerfusion". The FDA issued a decision of Substantially Equivalent on August 17, 2018. The device falls under product code OWB (Interventional Fluoroscopic X-Ray System), a Class II device regulated under 21 CFR 892.1650. Philips Medical Systems Nederlands B.V. has at least 7 other 510(k) clearances on record.