FDA 510(k) Applications Submitted by DAVID PHELPS

FDA 510(k) Number Submission Date Device Name Applicant
K960882 02/20/1996 CONTROL SYRINGE LOUISVILLE LABORATORIES, INC.
K963076 08/07/1996 LAPAROSCOPIC BONE ANCHORED URETHROPEXY INSTRUMENT TRAY LOUISVILLE LABORATORIES, INC.
K955535 12/05/1995 LOUISVILLE LABS OXYGEN HEAD TENT LOUISVILLE LABORATORIES, INC.


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