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PERCUTANEOUS DILATOR WITH SHEATH

Page Type
Cleared 510(K)
510(k) Number
K913932
510(k) Type
Traditional
Applicant
INTERVENTIONAL THERAPEUTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1991
Days to Decision
80 days
Submission Type
Statement

PERCUTANEOUS DILATOR WITH SHEATH

Page Type
Cleared 510(K)
510(k) Number
K913932
510(k) Type
Traditional
Applicant
INTERVENTIONAL THERAPEUTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1991
Days to Decision
80 days
Submission Type
Statement