FDA 510(k), K092560, PARI SINUS

FDA 510(k), K092560, PARI SINUS

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510(K) Number: K092560
Device Name: PARI SINUS
Manufacturer: PARI RESPIRATORY EQUIPMENT, INC.
Device Classification Name: nebulizer (direct patient interface)
Regulation Number: 868.5630
Classification Product Code: CAF
Date Received: 08/20/2009
Decision Date: 05/06/2010
Regulation Medical Specialty: Anesthesiology

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