FDA 510(k) Applications Submitted by GREGORY ALKIRE

FDA 510(k) Number Submission Date Device Name Applicant
K014294 12/28/2001 MODIFICATION TO ESCORT II+ 400 SERIES 9ESCORT PRISM) MONITOR, MODELS 20400, 20401, 20403, 20411, 20412, 20413, 20414 MEDICAL DATA ELECTRONICS
K012336 07/24/2001 MODIFICATION TO:ESCORT VISION CENTRAL STATION TELEMETRY SYSTEM, MODEL 20500 MEDICAL DATA ELECTRONICS


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