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EndoRotor Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN200016
510(k) Type
Direct
Applicant
Interscope, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
12/23/2020
Days to Decision
282 days

EndoRotor Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN200016
510(k) Type
Direct
Applicant
Interscope, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
12/23/2020
Days to Decision
282 days