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AMBULATORY EEG/SLEEP RECORDER AND ACCESSORIES, MODEL # SSR3201

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983072
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1998
Days to Decision
90 days
Submission Type
Summary

AMBULATORY EEG/SLEEP RECORDER AND ACCESSORIES, MODEL # SSR3201

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983072
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1998
Days to Decision
90 days
Submission Type
Summary