FDA 510(k) Applications Submitted by WILLIAM F GREENROSE
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K080040 |
01/07/2008 |
ORTHO ALL-FLEX DIAPHRAGM |
JOHNSON & JOHNSON PRODUTOS PROFISSIONAIS LTDA. |
K100104 |
01/13/2010 |
HYBERNITE RAINOUT CONTROL SYSTEM |
PLASTIFLEX GROUP NV |
K110246 |
01/27/2011 |
MEDISIZE RED AND MEDISIZE BLUE |
QSERVE AMERICA, INC. |
K070380 |
02/08/2007 |
PORTACLAMP FLEX |
CARDIO LIFE RESEARCH, S.A. |
K080621 |
03/05/2008 |
FASTLOCK, MODEL PC175M01, PC175MCE, PC005R01 |
EUROPEAN CUSTOM MANUFACTURING BV |
K060878 |
03/31/2006 |
GELITA-SPON ABSORBABLE GELATIN SPONGE, USP |
CURAMEDICAL, BV |
K111935 |
07/08/2011 |
TI-BASE ABUTMENT, 1 CONNECT ABUTMENT |
NT-TRADING GMBH AND CO KG |
K111988 |
07/13/2011 |
EASYSCAN MODEL 1.2 |
I-OPTICS BV |
K051911 |
07/14/2005 |
GELITA-SPON |
CURAMEDICAL, BV |
K112060 |
07/19/2011 |
RADIANCE |
GMV AEROSPACE AND DEFENCE S.A. |
K082556 |
09/04/2008 |
CLEARCORRECT |
CLEARCORRECT, INC. |
K082581 |
09/05/2008 |
C-QUEST |
MEDX, INC. |
K082594 |
09/08/2008 |
REMESENSE |
REMEDENT NV |
K102654 |
09/14/2010 |
VERTEX RAPID SIMPLIFIED |
VERTEX-DENTAL B.V. |
K082683 |
09/15/2008 |
SD CHECK GOLD |
STANDARD DIAGNOSTICS, INC. |
K083352 |
11/13/2008 |
VEINWAVE, TC3000 |
NEWLANDS CLINICAL TRIALS LTD |
K101123 |
04/22/2010 |
NEXFIN MODEL 2 |
BMEYE B.V. |
K091717 |
06/11/2009 |
ANY PLUS SPINAL FIXATION SYSTEM |
GS MEDICAL CO., LTD. |
K953616 |
08/03/1995 |
PREVIEW SURGERY PLANNING SOFTWARE |
MEDICAL MEDIA SYSTEMS |
K102640 |
09/14/2010 |
VERTEX SELF CURING, VERTEX CASTAVARIA, VERTEX CASTAPRESS |
VERTEX-DENTAL B.V. |
K092897 |
09/21/2009 |
LAP LOOP |
MEDSYS, S.A. |
K072834 |
10/03/2007 |
SIBEL SA VASCULAR CLAMP |
SURGICAL INSTRUMENTS BELGIUM SA |
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