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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