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ANGIOGRAPHIC CATHETER, MODEL ANGIOS

Page Type
Cleared 510(K)
510(k) Number
K092118
510(k) Type
Traditional
Applicant
Oscor Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2010
Days to Decision
183 days
Submission Type
Statement

ANGIOGRAPHIC CATHETER, MODEL ANGIOS

Page Type
Cleared 510(K)
510(k) Number
K092118
510(k) Type
Traditional
Applicant
Oscor Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2010
Days to Decision
183 days
Submission Type
Statement