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ACME GUIDEWIRES FOR PERCUTANEOUS INSERTION OF CATH

Page Type
Cleared 510(K)
510(k) Number
K883763
510(k) Type
Traditional
Applicant
ACME-MONACO CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1988
Days to Decision
73 days

ACME GUIDEWIRES FOR PERCUTANEOUS INSERTION OF CATH

Page Type
Cleared 510(K)
510(k) Number
K883763
510(k) Type
Traditional
Applicant
ACME-MONACO CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1988
Days to Decision
73 days