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PHILLIPS OMNIDIAGNOST ELEVA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032046
510(k) Type
Traditional
Applicant
Philips Medical Systems, Inc.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
7/17/2003
Days to Decision
15 days
Submission Type
Summary

PHILLIPS OMNIDIAGNOST ELEVA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032046
510(k) Type
Traditional
Applicant
Philips Medical Systems, Inc.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
7/17/2003
Days to Decision
15 days
Submission Type
Summary