510(k) K811142

BELMONT PODIATRY MODEL 065 X-RAY by Belmont Equipment Corp. — Product Code KPR

K811142 is an FDA 510(k) premarket notification submitted by Belmont Equipment Corp. for the device "BELMONT PODIATRY MODEL 065 X-RAY". The FDA issued a decision of Substantially Equivalent on June 9, 1981. The device falls under product code KPR (System, X-Ray, Stationary), a Class II device regulated under 21 CFR 892.1680. Belmont Equipment Corp. has at least 10 other 510(k) clearances on record.