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CANDELA DIRECTABLE BILIARY CATHETER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K900904
510(k) Type
Traditional
Applicant
CANDELA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1990
Days to Decision
73 days

CANDELA DIRECTABLE BILIARY CATHETER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K900904
510(k) Type
Traditional
Applicant
CANDELA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1990
Days to Decision
73 days