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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