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FDA 510(k) Applications Submitted by DIGITEC MEDICAL SERVICE CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K993681
11/01/1999
DIGITEC TWO STAGE COMPRESSION KIT
DIGITEC MEDICAL SERVICE CORP.
K010792
03/16/2001
MAMMOGRAPH
DIGITEC MEDICAL SERVICE CORP.
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