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NIHON KOHDEN BSM-2300A SERIES BEDSIDE MONITOR AND ACCESSORIES, MODEL BSM-2300A SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011918
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2001
Days to Decision
84 days
Submission Type
Summary

NIHON KOHDEN BSM-2300A SERIES BEDSIDE MONITOR AND ACCESSORIES, MODEL BSM-2300A SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011918
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2001
Days to Decision
84 days
Submission Type
Summary