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HORTMANN ECHOMASTER OAE ANALYZER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994033
510(k) Type
Traditional
Applicant
Hortmann AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2000
Days to Decision
90 days
Submission Type
Statement

HORTMANN ECHOMASTER OAE ANALYZER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994033
510(k) Type
Traditional
Applicant
Hortmann AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2000
Days to Decision
90 days
Submission Type
Statement