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FUKUDA DENSHI DYNASCOPE MODEL DS-7000/7000M PATIENT MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081891
510(k) Type
Traditional
Applicant
FUKUDA DENSHI USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2008
Days to Decision
58 days
Submission Type
Summary

FUKUDA DENSHI DYNASCOPE MODEL DS-7000/7000M PATIENT MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081891
510(k) Type
Traditional
Applicant
FUKUDA DENSHI USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2008
Days to Decision
58 days
Submission Type
Summary