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Reconnaissance PV .018 OTW Digital IVUS Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200410
510(k) Type
Traditional
Applicant
Philips Image Guided Therapy Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2020
Days to Decision
93 days
Submission Type
Summary

Reconnaissance PV .018 OTW Digital IVUS Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200410
510(k) Type
Traditional
Applicant
Philips Image Guided Therapy Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2020
Days to Decision
93 days
Submission Type
Summary