FDA 510(k) Applications Submitted by KRONNER PROTOTYPES, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K973543 09/18/1997 KRONNER LOW PROFILE SCOPE HOLDER KRONNER PROTOTYPES, INC.
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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