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VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIES

Page Type
Cleared 510(K)
510(k) Number
K000457
510(k) Type
Traditional
Applicant
RETINALABS.COM
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2000
Days to Decision
88 days
Submission Type
Summary

VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIES

Page Type
Cleared 510(K)
510(k) Number
K000457
510(k) Type
Traditional
Applicant
RETINALABS.COM
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2000
Days to Decision
88 days
Submission Type
Summary