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AltaTrack equipment, AltaTrack Guidewire, AltaTrack Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201081
510(k) Type
Traditional
Applicant
Philips Medical System Nederland B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
12/17/2020
Days to Decision
239 days
Submission Type
Summary

AltaTrack equipment, AltaTrack Guidewire, AltaTrack Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201081
510(k) Type
Traditional
Applicant
Philips Medical System Nederland B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
12/17/2020
Days to Decision
239 days
Submission Type
Summary