FDA 510(k) Applications Submitted by RONALD R MANNA

FDA 510(k) Number Submission Date Device Name Applicant
K070779 03/21/2007 SONATHERM 600I ULTRASONIC LESION GENERATING SYSTEM MISONIX, INC.
K123980 12/26/2012 SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIES MISONIX, INC.
K070313 02/01/2007 MISONIX, INC., AUSS-7 ULTRASONIC SURGICAL ASPIRATOR SYSTEM MISONIX, INC.
K050776 03/28/2005 AUSS-6 ULTRASONIC SURGICAL ASPIRATOR SYSTEM MISONIX, INC.
K041058 04/23/2004 MISONIX INC. LYSONIX 2000/3000 ULTRASONIC SURGICAL ASPIRATOR SYSTEMS MISONIX, INC.
K042096 08/04/2004 MISONIX INC. SONATHERM 600 ULTRASONIC LESION GENERATING SYSTEM MISONIX, INC.
K062471 08/24/2006 ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL FS 1000 RF MISONIX, INC.
K032690 09/02/2003 MISONIX INC. FS 1000 RF ULTRASONIC SURGICAL ASPIRATOR SYSTEM MISONIX, INC.
K112782 09/26/2011 MISONIX SONICONE(R) ULTRASONIC WOUND CARE SYSTEM AND ACCESSORIES MISONIX, INC.
K052702 09/28/2005 MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORY MISONIX, INC.


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