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FDA 510(k) Applications Submitted by MERIDIAN MEDICAL TECHNOLOGIES, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030104
01/13/2003
PRIME ECG SYSTEM
MERIDIAN MEDICAL TECHNOLOGIES, INC.
K012414
07/30/2001
PRIME ECG SYSTEM
MERIDIAN MEDICAL TECHNOLOGIES, INC.
K965101
12/20/1996
CARDIOBEEPER CB-12L
MERIDIAN MEDICAL TECHNOLOGIES, INC.
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