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SPYGLASS ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K962805
510(k) Type
Traditional
Applicant
DAIG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/1996
Days to Decision
89 days
Submission Type
Statement

SPYGLASS ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K962805
510(k) Type
Traditional
Applicant
DAIG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/1996
Days to Decision
89 days
Submission Type
Statement