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VYNTUS/ SENTRYSUITE PRODUCT LINE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133925
510(k) Type
Traditional
Applicant
CAREFUSION GERMANY 234 GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/22/2014
Days to Decision
242 days
Submission Type
Summary

VYNTUS/ SENTRYSUITE PRODUCT LINE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133925
510(k) Type
Traditional
Applicant
CAREFUSION GERMANY 234 GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/22/2014
Days to Decision
242 days
Submission Type
Summary