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NES Reprocessed Eagle Eye Platinum RX Digital IVUS Catheter

Page Type
Cleared 510(K)
510(k) Number
K223026
510(k) Type
Traditional
Applicant
Northeast Scientific, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/2023
Days to Decision
127 days
Submission Type
Summary

NES Reprocessed Eagle Eye Platinum RX Digital IVUS Catheter

Page Type
Cleared 510(K)
510(k) Number
K223026
510(k) Type
Traditional
Applicant
Northeast Scientific, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/2023
Days to Decision
127 days
Submission Type
Summary