FDA 510(k) Applications Submitted by LORETTA LUHMAN

FDA 510(k) Number Submission Date Device Name Applicant
K962042 05/28/1996 GLASS SYRINGE ISPG, INC.
K962886 07/24/1996 ANESTHESIA CONDUCTION NEEDLE ISPG, INC.
K012358 07/25/2001 CHIBA NEEDLE ISPG, INC.


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