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FDA 510(k) Applications Submitted by GERHARDT SEIWERTH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K010714
03/09/2001
EXPANDER, MODELS 1400880, 1401280, 1401680, 1401880, 1410420, 1410620, 1410830
MEDI-GLOBE CORP.
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