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LARYNGOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K912905
510(k) Type
Traditional
Applicant
ACORN GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/1991
Days to Decision
90 days
Submission Type
Statement

LARYNGOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K912905
510(k) Type
Traditional
Applicant
ACORN GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/1991
Days to Decision
90 days
Submission Type
Statement