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Reconnaissance PV .018 OTW Digital IVUS Catheter

Page Type
Cleared 510(K)
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)
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