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FDA 510(k) Applications Submitted by DAVID M 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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