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NEURORECOVERY VENTRICULAR CATHETER & MAIN VALVE ASSEMBLY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022638
510(k) Type
Traditional
Applicant
NEURORECOVERY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2002
Days to Decision
84 days
Submission Type
Summary

NEURORECOVERY VENTRICULAR CATHETER & MAIN VALVE ASSEMBLY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022638
510(k) Type
Traditional
Applicant
NEURORECOVERY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2002
Days to Decision
84 days
Submission Type
Summary