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FDA 510(k) Applications Submitted by ROBERT SCHREIBER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K031356
04/11/2003
HEMAPROMPT GASTRIC
AERSCHER DIAGNOSTICS
K981661
05/06/1998
HEMAPROMPT
AERSCHER DIAGNOSTICS
K972763
07/24/1997
HEMAPROMPT
AERSCHER DIAGNOSTICS
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