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FDA 510(k) Applications Submitted by DALE COLEMAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990041
01/06/1999
UROSTYM BIOFEEDBACK AND STIMULATION PROBES
LABORIE MEDICAL TECH CORP.
K960512
02/05/1996
GEMINI PC-ITX
IMED CORP.
K991479
04/28/1999
VISER PENILE TUMESCENCE MONITOR
LABORIE MEDICAL TECH CORP.
K993721
11/03/1999
UROSTYM BIOFEEDBACK AND STIMULATION ANAL/RECTAL PROBES
LABORIE MEDICAL TECH CORP.
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