Last synced on 30 September 2022 at 11:05 pm

NEUROREADER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950986
510(k) Type
Traditional
Applicant
ARTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/1995
Days to Decision
251 days
Submission Type
Statement

NEUROREADER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950986
510(k) Type
Traditional
Applicant
ARTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/1995
Days to Decision
251 days
Submission Type
Statement