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FDA 510(k) Applications Submitted by LOCKETT MEDICAL CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K954887
10/16/1995
STERILE WATER O.9% STERILE SALINE
LOCKETT MEDICAL CORP.
K011176
04/17/2001
REUSABLE GLASS SYRINGES
LOCKETT MEDICAL CORP.
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