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FDA 510(k) Applications Submitted by RICHARD F KRONNER, M.D.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K000663
02/28/2000
KRONNER LOW PROFILE SCOPE HOLDER
KRONNER PROTOTYPES, INC.
K130758
03/20/2013
KRONNER SIDE-KICK UTERINE MANIPULATOR HOLDER
KRONNER PROTOTYPES, INC.
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