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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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