FDA 510(k) Applications Submitted by AERSCHER DIAGNOSTICS

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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