AQUABEAM System

Fluid Jet Removal System

PROCEPT BioRobotics Corporation

The following data is part of a De Novo classification by Procept Biorobotics Corporation with the FDA for Aquabeam System.

Pre-market Notification Details

DeNovo IDDEN170024
Device Name:AQUABEAM System
ClassificationFluid Jet Removal System
Applicant PROCEPT BioRobotics Corporation 900 Island Drive Suite 101 Redwood Shores,  CA  94568
ContactMichael Nketiah
Product CodePZP  
CFR Regulation Number876.4350 [🔎]
DecisionGranted (DENG)
510(k) Premarket NotificationDevice Classification Under Section 513(f)(2)(de Novo) // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Lin
Review Advisory BoardGastroenterology/Urology
Classification AdvisoryGeneral & Plastic Surgery
TypeDirect
Date Received2017-04-17
Decision Date2017-12-21
FDA ReviewDecision Summary
Reclassification Order:Reclassification Order

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
B614AB2000 DEN170024 000
B6143103011 DEN170024 000
B6142105011 DEN170024 000
B6142101011 DEN170024 000
B614SC20000 DEN170024 000
00850055427020 DEN170024 000

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