FDA 510(k) Applications Submitted by DAVID HIMES

FDA 510(k) Number Submission Date Device Name Applicant
K990038 01/06/1999 HUMMER TRAK SYSTEM Stryker Endoscopy
K001492 05/12/2000 QUINTON Q-STRESS, MODEL 000483 QUINTON, INC.
K003576 11/20/2000 Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503 QUINTON, INC.


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