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FDA 510(k) Applications Submitted by CHRISTOPHER B KNELL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K991872
06/01/1999
LYNX ULTRASOUND SYSTEM
ECTON, INC.
K982800
08/10/1998
ECTON LYNX ULTRASOUND SYSTEM
ECTON, INC.
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