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NIHON KOHDEN EEG-1200A SERIES NEUROFAX, MODEL EEG-1200A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080546
510(k) Type
Special
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2008
Days to Decision
183 days
Submission Type
Summary

NIHON KOHDEN EEG-1200A SERIES NEUROFAX, MODEL EEG-1200A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080546
510(k) Type
Special
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2008
Days to Decision
183 days
Submission Type
Summary