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ENDOSCOPIC VENTRICULAR CATHETER

Page Type
Cleared 510(K)
510(k) Number
K971617
510(k) Type
Traditional
Applicant
INTEGRA NEUROCARE LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/1997
Days to Decision
90 days
Submission Type
Statement

ENDOSCOPIC VENTRICULAR CATHETER

Page Type
Cleared 510(K)
510(k) Number
K971617
510(k) Type
Traditional
Applicant
INTEGRA NEUROCARE LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/1997
Days to Decision
90 days
Submission Type
Statement