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FDA 510(k) Applications Submitted by CAROLYN ANDERSON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K040345
02/12/2004
MODIFICATION TO NITREX NITINOL GUIDEWIRE
EV3 INC
K060774
03/22/2006
FOLATE ON THE ACCESS IMMUNOASSAY SYSTEMS, MODEL A14208
BECKMAN COULTER, INC.
K991114
04/01/1999
REGULAR DIAMETER SINGLE STAGE (RDS) TPS DENTAL IMPLANT SYSTEM
LIFECORE BIOMEDICAL, INC.
K031864
06/16/2003
NITREX NITINOL GUIDEWIRE
EV3 CORPORATION
K002037
07/05/2000
LIFECORE BIOMEDICAL DENTAL IMPLANT SYSTEMS
LIFECORE BIOMEDICAL, INC.
K052082
08/02/2005
FERRITIN ON THE ACCESS IMMUNOASSAY SYSTEMS, MODEL 33020
BECKMAN COULTER, INC.
K003226
10/16/2000
THE LIFECORE STAGE-1 SINGLE STAGE RBM DENTAL IMPLANT SYSTEM
LIFECORE BIOMEDICAL, INC.
K993894
11/16/1999
LIFECORE SINGLE TOOTH ABUTMENT SYSTEM
LIFECORE BIOMEDICAL, INC.
K994205
12/01/1999
MODIFICATION OF REGULAR DIAMETER SINGLE STAGE (RDS) TPS DENTAL IMPLANT SYSTEM
LIFECORE BIOMEDICAL, INC.
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