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Miethke Shunt System GAV 2.0 and SA 2.0 Valves

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190174
510(k) Type
Traditional
Applicant
Aesculap, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2019
Days to Decision
154 days
Submission Type
Summary

Miethke Shunt System GAV 2.0 and SA 2.0 Valves

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190174
510(k) Type
Traditional
Applicant
Aesculap, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2019
Days to Decision
154 days
Submission Type
Summary