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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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