510(k) K991113

`INEAR WRIST COIL, MODEL 440GE-09 by Medical Advances, Inc. — Product Code MOS

K991113 is an FDA 510(k) premarket notification submitted by Medical Advances, Inc. for the device "`INEAR WRIST COIL, MODEL 440GE-09". The FDA issued a decision of Substantially Equivalent on Jun 10, 1999. The device falls under product code MOS (Coil, Magnetic Resonance, Specialty), a Class II device regulated under 21 CFR 892.1000. Medical Advances, Inc. has 56 other 510(k) clearances on record.