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ACCUTECH FAMILY OF POWERFLEX LASER DELIVERY DEVICES

Page Type
Cleared 510(K)
510(k) Number
K090281
510(k) Type
Traditional
Applicant
ACCUTECH MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2009
Days to Decision
27 days
Submission Type
Summary

ACCUTECH FAMILY OF POWERFLEX LASER DELIVERY DEVICES

Page Type
Cleared 510(K)
510(k) Number
K090281
510(k) Type
Traditional
Applicant
ACCUTECH MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2009
Days to Decision
27 days
Submission Type
Summary