FDA 510(k) Applications Submitted by DAVID GARVIN

FDA 510(k) Number Submission Date Device Name Applicant
K001017 03/29/2000 RETRAX RETRACTING NEEDLE SYRINGE, SIZE 3CC RETRAX SAFETY SYSTEMS, INC.
K031394 05/02/2003 AMERICAN SYRINGE COMPANY 1CC AND 3CC SYRINGE AMERICAN SYRINGE COMPANY


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