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ANGIOGRAPHIC CATHETER -- MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K922101
510(k) Type
Traditional
Applicant
INTERVENTIONAL THERAPEUTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1993
Days to Decision
282 days
Submission Type
Statement

ANGIOGRAPHIC CATHETER -- MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K922101
510(k) Type
Traditional
Applicant
INTERVENTIONAL THERAPEUTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1993
Days to Decision
282 days
Submission Type
Statement