510(k) K914536

MODELS 190GE-64/191GE-64/192GE-64/193GE-64 by Medical Advances, Inc. — Product Code LNH

K914536 is an FDA 510(k) premarket notification submitted by Medical Advances, Inc. for the device "MODELS 190GE-64/191GE-64/192GE-64/193GE-64". The FDA issued a decision of Substantially Equivalent on Nov 27, 1991. The device falls under product code LNH (System, Nuclear Magnetic Resonance Imaging), a Class II device regulated under 21 CFR 892.1000. Medical Advances, Inc. has 56 other 510(k) clearances on record.