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FDA 510(k) Applications Submitted by SRS MEDICAL SYSTEMS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K002834
09/12/2000
SRS VAGINAL EMG/STIMULATION PERINEOMETER SENSOR SRS ANAL EMG/STIMULATION PERINEOMETER SENSOR
SRS MEDICAL SYSTEMS, INC.
K003127
10/06/2000
REGAIN DESKTOP
SRS MEDICAL SYSTEMS, INC.
K003367
10/30/2000
ORION PLATINUM
SRS MEDICAL SYSTEMS, INC.
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