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FDA 510(k) Applications Submitted by ISPG, INC.
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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