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CANDELA MINI-UB ENDOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K910732
510(k) Type
Traditional
Applicant
CANDELA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/1991
Days to Decision
50 days

CANDELA MINI-UB ENDOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K910732
510(k) Type
Traditional
Applicant
CANDELA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/1991
Days to Decision
50 days