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FDA 510(k)

RZ Resectoscope System

K-Number: K243382 · 2025-06-03

ApplicantRz Medizintechnik GmbH
Decision Date2025-06-03
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

RZ Resectoscope System is a medical device manufactured by Rz Medizintechnik GmbH. It received FDA 510(k) clearance on 2025-06-03 under approval number K243382. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RZ Resectoscope System?

RZ Resectoscope System is a medical device that received FDA 510(k) clearance on 2025-06-03. It is manufactured by Rz Medizintechnik GmbH. The 510(k) number is K243382.

When was RZ Resectoscope System approved by the FDA?

RZ Resectoscope System received FDA 510(k) clearance on 2025-06-03, under approval number K243382.

What company makes RZ Resectoscope System?

RZ Resectoscope System is manufactured by Rz Medizintechnik GmbH.

What is the FDA product code for RZ Resectoscope System?

The FDA product code for RZ Resectoscope System is HIH.

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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.

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