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CORONARY GUIDE WIRE

Page Type
Cleared 510(K)
510(k) Number
K883579
510(k) Type
Traditional
Applicant
DATASCOPE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1988
Days to Decision
74 days

CORONARY GUIDE WIRE

Page Type
Cleared 510(K)
510(k) Number
K883579
510(k) Type
Traditional
Applicant
DATASCOPE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1988
Days to Decision
74 days