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VISIRASER

Page Type
Cleared 510(K)
510(k) Number
K904126
510(k) Type
Traditional
Applicant
ACORN GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1990
Days to Decision
54 days

VISIRASER

Page Type
Cleared 510(K)
510(k) Number
K904126
510(k) Type
Traditional
Applicant
ACORN GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1990
Days to Decision
54 days