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FDA 510(k) Applications Submitted by LES PADILLA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030405
02/06/2003
QMS / MULTIGENT VALPROIC ACID REAGENT, PART #396075
SERADYN
K033674
11/24/2003
MULTIGENT HEMOGLOBIN A1C (REAGENTS), HB A1C CALIBRATORS AND HB A1C CONTROLS
SERADYN INC.
K093312
10/22/2009
KIMBERLY-CLARK GASTROINTESTINAL ANCHOR SET WITH SAF-T-PEXY FASTENERS, ENTERNAL ACCESS DILATION SYSTEM
KIMBERLY-CLARK CORP.
K060121
01/17/2006
BIOMET PRE-CALIBRATED COMPUTER AIDED SURGERY NAVIGATION INSTRUMENTS FOR HIP APPLICATIONS
BIOMET MANUFACTURING CORP.
K060693
03/15/2006
MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR
ARTHROTEK, INC.
K061340
05/15/2006
23 MM SINGLE-PEG PATELLA COMPONENT
BIOMET MANUFACTURING, INC.
K061389
05/18/2006
ALLTHREAD LACTOSORB SUTURE ANCHOR
ARTHROTEK, INC.
K101596
06/08/2010
KIMBERLY-CLARK PURPLE NITRILE POWDER-FREE EXAM GLOVE (CHEMOTHERAPY GLOVE) AND KIMBERLY-CLARK PURPLE NITRILE XTRA POWDER-
KIMBERLY-CLARK
K061657
06/13/2006
HITCH LACTOSORB SUTURE ANCHOR
ARTHROTEK, INC.
K061681
06/15/2006
REPICCI II METAL BACK INLAY UNICOMPARTMENTAL TIBIAL BEARING COMPONENT
BIOMET MANUFACTURING CORP.
K102032
07/19/2010
KIMBERLY-CLARK PURPLE NITRILE XTRA* STERILE POWDER-FREE EXAM GLOVE (CHEMOTHERAPY GLOVE) - 12 STERILE PAIRS
KIMBERLY-CLARK CORP.
K052990
10/24/2005
STAGEONE DISPOSABLE CEMENT SPACER MOLD FOR TEMPORARY HIP PROSTHESIS WITH REINFORCEMENT STEM
BIOMET, INC.
K113423
11/21/2011
KIMBERLY CLARK PURPLE NITRILE, AND PURPLE NITRILE XTRA POWDER FREE EXAM GLOVE
KIMBERLY-CLARK CORP.
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