510(k) K014056

SALTER LABS MODIFIED NEBUTECH NEBULIZER by Salter Labs — Product Code CAF

K014056 is an FDA 510(k) premarket notification submitted by Salter Labs for the device "SALTER LABS MODIFIED NEBUTECH NEBULIZER". The FDA issued a decision of Substantially Equivalent on February 1, 2002. The device falls under product code CAF (Nebulizer (Direct Patient Interface)), a Class II device regulated under 21 CFR 868.5630. Salter Labs has at least 10 other 510(k) clearances on record.