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CAROTID BYPASS SHUNT WITH SAMPLING ARM

Page Type
Cleared 510(K)
510(k) Number
K860743
510(k) Type
Traditional
Applicant
CLINCAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1986
Days to Decision
90 days

CAROTID BYPASS SHUNT WITH SAMPLING ARM

Page Type
Cleared 510(K)
510(k) Number
K860743
510(k) Type
Traditional
Applicant
CLINCAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1986
Days to Decision
90 days