FDA 510(k) Applications Submitted by ROBERT WAGNER
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K130225 |
01/29/2013 |
QUASAR C100, BABY QUASAR PLUS, QUASAR MD PLUS; WRINKLE REDUCTION DEVICE |
SILVERBAY LLC, D/B/A QUASAR BIO-TECH |
K111049 |
04/15/2011 |
MOBILE VERSA LIGHT |
MEDTEK LIGHTING CORP |
K111286 |
05/06/2011 |
QUASAR CALYPSO |
SILVER BAY, LLC |
K092435 |
08/07/2009 |
VERSEO AIR PRESSURE MASSAGER |
THE AMERICAN EXPORT GROUP & INTERNATIONAL SERVICES |
K112362 |
08/17/2011 |
C100 WRINKLE REDUCTION DEVICE |
SILVER BAY, LLC |
K040905 |
04/07/2004 |
WELLNESS/JOLIVETE |
TOHKAI PRECISION IND. LTD. |
K101190 |
04/28/2010 |
LIGHTSTIM ANTI-WRINKLE OTC MODEL AAL OTC |
LED INTELLECTUAL PROPERTIES, LLC |
K051330 |
05/20/2005 |
UVBIOTEK MODELS 3200B AND 4000B |
MEDTEK LIGHTING CORPORATION |
K022626 |
08/07/2002 |
MOISTURESTAY (REVLON) |
RAYMOND INDUSTRIAL, LTD. |
K092800 |
09/11/2009 |
ANTI-WRINKLE (AGING) LIGHT, MODEL AAL |
LED INTELLECTUAL PROPERTIES, LLC |
K083580 |
12/03/2008 |
ANTI-WRINKLE LIGHT, MODEL 1302 AND PAIN THERAPY LIGHT, MODEL 1301 |
LED INTELLECTUAL PROPERTIES, LLC |
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