Last synced on 14 June 2024 at 11:05 pm

NIHON KOHDEN ELECTROENCEPHALOGRAPH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944678
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/1995
Days to Decision
242 days
Submission Type
Summary

NIHON KOHDEN ELECTROENCEPHALOGRAPH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944678
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/1995
Days to Decision
242 days
Submission Type
Summary