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ACCULASER PRO LOW LEVEL LASER THERAPY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K020657
510(k) Type
Traditional
Applicant
ACCULASER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2002
Days to Decision
151 days
Submission Type
Summary

ACCULASER PRO LOW LEVEL LASER THERAPY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K020657
510(k) Type
Traditional
Applicant
ACCULASER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2002
Days to Decision
151 days
Submission Type
Summary