FDA 510(k) Applications Submitted by Genesee BioMedical, Inc.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K093903 |
12/22/2009 |
ATS TRI-AD SEMI-FLEXIBLE TRICUSPID ANUULOPLASTY, MODEL 900SFC |
Genesee BioMedical, Inc. |
K090428 |
02/19/2009 |
ATS SIMULUS ADJUSTABLE FLEXIBLE ANNULOPLASTY, MODEL 735 AC |
Genesee BioMedical, Inc. |
K071214 |
05/01/2007 |
ATS SIMULUS ADJUSTABLE FLEXIBLE ANNULOPLASTY RING |
Genesee BioMedical, Inc. |
K072655 |
09/20/2007 |
ATS SIMULUS SEMI-RIGID MITRAL ANNULOPLASTY RING, MODEL 800SR |
Genesee BioMedical, Inc. |
K052565 |
09/19/2005 |
ATS SIMULUS ANNULOPLASTY RING, MODEL 700FF |
Genesee BioMedical, Inc. |
K052899 |
10/14/2005 |
ATS SIMULUS ANNULOPLASTY BAND, MODEL 700FC |
Genesee BioMedical, Inc. |
K083683 |
12/12/2008 |
ATS SIMULUS SEMI-RIGID MITRAL ANNULOPLASTY RING, MODEL 800SC |
Genesee BioMedical, Inc. |
K161815 |
07/01/2016 |
FlexForm Annuloplasty Ring and FlexForm Annuloplasty Band |
Genesee BioMedical, Inc. |
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