Last synced on 14 June 2024 at 11:05 pm

CUEVA CRANIAL NERVE ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944061
510(k) Type
Traditional
Applicant
AD-TECH MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/1995
Days to Decision
154 days
Submission Type
Statement

CUEVA CRANIAL NERVE ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944061
510(k) Type
Traditional
Applicant
AD-TECH MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/1995
Days to Decision
154 days
Submission Type
Statement