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Fukuda Denshi DynaScope Model DS-8000 Series Patient Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150030
510(k) Type
Traditional
Applicant
Fukuda Denshi USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2015
Days to Decision
67 days
Submission Type
Summary

Fukuda Denshi DynaScope Model DS-8000 Series Patient Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150030
510(k) Type
Traditional
Applicant
Fukuda Denshi USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2015
Days to Decision
67 days
Submission Type
Summary