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NIHON KOHDEN AE-918P NEURO UNIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130238
510(k) Type
Traditional
Applicant
NIHON KOHDEN CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2015
Days to Decision
762 days
Submission Type
Summary

NIHON KOHDEN AE-918P NEURO UNIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130238
510(k) Type
Traditional
Applicant
NIHON KOHDEN CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2015
Days to Decision
762 days
Submission Type
Summary