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AQUABEAM System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN170024
510(k) Type
Direct
Applicant
Procept Biorobotics, Corporation
Country
United States
FDA Decision
Deleted
Decision Date
12/21/2017
Days to Decision
248 days

AQUABEAM System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN170024
510(k) Type
Direct
Applicant
Procept Biorobotics, Corporation
Country
United States
FDA Decision
Deleted
Decision Date
12/21/2017
Days to Decision
248 days