Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HYDROS Robotic System; HYDROS TRUS Probe; HYDROS Handpiece

K-Number: K240200 · 2024-08-20

Decision Date2024-08-20
Product CodePZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HYDROS Robotic System; HYDROS TRUS Probe; HYDROS Handpiece is a medical device manufactured by Procept Biorobotics. It received FDA 510(k) clearance on 2024-08-20 under approval number K240200. The device is classified under product code PZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDROS Robotic System; HYDROS TRUS Probe; HYDROS Handpiece?

HYDROS Robotic System; HYDROS TRUS Probe; HYDROS Handpiece is a medical device that received FDA 510(k) clearance on 2024-08-20. It is manufactured by Procept Biorobotics. The 510(k) number is K240200.

When was HYDROS Robotic System; HYDROS TRUS Probe; HYDROS Handpiece approved by the FDA?

HYDROS Robotic System; HYDROS TRUS Probe; HYDROS Handpiece received FDA 510(k) clearance on 2024-08-20, under approval number K240200.

What company makes HYDROS Robotic System; HYDROS TRUS Probe; HYDROS Handpiece?

HYDROS Robotic System; HYDROS TRUS Probe; HYDROS Handpiece is manufactured by Procept Biorobotics.

What is the FDA product code for HYDROS Robotic System; HYDROS TRUS Probe; HYDROS Handpiece?

The FDA product code for HYDROS Robotic System; HYDROS TRUS Probe; HYDROS Handpiece is PZP.

Related Clinical Trials

Related PubMed Literature

Other Devices by Procept Biorobotics

Related Devices (Code: PZP)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.