Last synced on 19 July 2024 at 11:05 pm

LARYNGOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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