Last synced on 30 September 2022 at 11:05 pm

MEDI-DX 7000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964622
510(k) Type
Traditional
Applicant
NEURO-DIAGNOSTIC ASSOC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1997
Days to Decision
378 days
Submission Type
Summary

MEDI-DX 7000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964622
510(k) Type
Traditional
Applicant
NEURO-DIAGNOSTIC ASSOC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1997
Days to Decision
378 days
Submission Type
Summary