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CANDELA RETINAL CAMERA

Page Type
Cleared 510(K)
510(k) Number
K913314
510(k) Type
Traditional
Applicant
CANDELA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/1992
Days to Decision
182 days
Submission Type
Summary

CANDELA RETINAL CAMERA

Page Type
Cleared 510(K)
510(k) Number
K913314
510(k) Type
Traditional
Applicant
CANDELA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/1992
Days to Decision
182 days
Submission Type
Summary