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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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