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FDA 510(k) Applications Submitted by HORTMANN AG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K980505
02/09/1998
HORTMANN AMDIS-OAE OAE ANALYZER
HORTMANN AG
K994033
11/26/1999
HORTMANN ECHOMASTER OAE ANALYZER
HORTMANN AG
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