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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