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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