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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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