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FDA 510(k) Applications Submitted by ROBERT KRIEDERMANN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990066
01/08/1999
CCD CAMERA, MODEL 9000
CAMTRONICS, LTD.
K992259
07/06/1999
ECHOCARDIOGRAPHY SYSTEM SERIES 95000
CAMTRONICS, LTD.
K992666
08/09/1999
VIDEO PLUS SYSTEM, SERIES 95000
CAMTRONICS, LTD.
K955519
12/04/1995
ANALYTICAL REVIEW STATION
CAMTRONICS, LTD.
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