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Lumix Ultra 1, Lumix Ultra 2, Lumix Ultra 3

Page Type
Cleared 510(K)
510(k) Number
K161198
510(k) Type
Traditional
Applicant
USA LASER BIOTECH INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2016
Days to Decision
89 days
Submission Type
Summary

Lumix Ultra 1, Lumix Ultra 2, Lumix Ultra 3

Page Type
Cleared 510(K)
510(k) Number
K161198
510(k) Type
Traditional
Applicant
USA LASER BIOTECH INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2016
Days to Decision
89 days
Submission Type
Summary