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NES Reprocessed Visions PV .014P RX Digital IVUS Catheter

Page Type
Cleared 510(K)
510(k) Number
K200195
510(k) Type
Traditional
Applicant
Northeast Scientific, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2020
Days to Decision
147 days
Submission Type
Summary

NES Reprocessed Visions PV .014P RX Digital IVUS Catheter

Page Type
Cleared 510(K)
510(k) Number
K200195
510(k) Type
Traditional
Applicant
Northeast Scientific, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2020
Days to Decision
147 days
Submission Type
Summary