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Ventricular Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200950
510(k) Type
Special
Applicant
Aesculap, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2020
Days to Decision
29 days
Submission Type
Summary

Ventricular Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200950
510(k) Type
Special
Applicant
Aesculap, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2020
Days to Decision
29 days
Submission Type
Summary