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Stimuplex Onvision System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192914
510(k) Type
Traditional
Applicant
Philips Medical Systems Nederland B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
5/27/2020
Days to Decision
225 days
Submission Type
Summary

Stimuplex Onvision System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192914
510(k) Type
Traditional
Applicant
Philips Medical Systems Nederland B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
5/27/2020
Days to Decision
225 days
Submission Type
Summary