FDA 510(k) Applications Submitted by AMERICAN DIAGNOSTIC CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K962655 07/08/1996 ANEROID AND MERCURIAL SPHYGMOMANOMETERS AMERICAN DIAGNOSTIC CORP.
K012304 07/20/2001 ADC 656 ELECTRONIC STETHOSCOPE AMERICAN DIAGNOSTIC CORP.
K060321 02/09/2006 ADSCOPE 657BK ELECTRONIC STETHOSCOPE, MODEL 657BK AMERICAN DIAGNOSTIC CORP.
K162589 09/16/2016 Adscope 658 Electronic Stethoscope AMERICAN DIAGNOSTIC CORP.
K093495 11/10/2009 OTOSCOPE AND OPHTHALMOSCOPE DIAGNOSTIC INSTRUMENT KITS AMERICAN DIAGNOSTIC CORP.


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