510(k) K760221

I.P.P.B., DIS. W/MANIFOLD/NEBULIZER by Manner Medical Products — Product Code CBO

K760221 is an FDA 510(k) premarket notification submitted by Manner Medical Products for the device "I.P.P.B., DIS. W/MANIFOLD/NEBULIZER". The FDA issued a decision of Substantially Equivalent on August 3, 1976. The device falls under product code CBO (Attachment, Intermittent Mandatory Ventilation (Imv)), a Class II device regulated under 21 CFR 868.5955. Manner Medical Products has at least 3 other 510(k) clearances on record.