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PHILIPS OMNIDIAGNOST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982993
510(k) Type
Traditional
Applicant
Philips Medical Systems, Inc.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
9/29/1998
Days to Decision
33 days
Submission Type
Summary

PHILIPS OMNIDIAGNOST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982993
510(k) Type
Traditional
Applicant
Philips Medical Systems, Inc.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
9/29/1998
Days to Decision
33 days
Submission Type
Summary