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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