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FUKUDA DENSHI DYNASCOPE MODEL DS-7000 SERIES PATIENT MONITOR, MODEL DS-7000//7000M/7210/7210M

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083697
510(k) Type
Traditional
Applicant
FUKUDA DENSHI USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2009
Days to Decision
94 days
Submission Type
Summary

FUKUDA DENSHI DYNASCOPE MODEL DS-7000 SERIES PATIENT MONITOR, MODEL DS-7000//7000M/7210/7210M

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083697
510(k) Type
Traditional
Applicant
FUKUDA DENSHI USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2009
Days to Decision
94 days
Submission Type
Summary