HYDROS Robotic System; HYDROS TRUS Probe; HYDROS Handpiece
K-Number: K240200 · 2024-08-20
Device Summary
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.
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Related PubMed Literature
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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.