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FDA 510(k)

KARL STORZ ICG Imaging System

K-Number: K232857 · 2023-11-06

Decision Date2023-11-06
Product CodeOWN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KARL STORZ ICG Imaging System is a medical device manufactured by Karl Storz SE & CO. KG. It received FDA 510(k) clearance on 2023-11-06 under approval number K232857. The device is classified under product code OWN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ ICG Imaging System?

KARL STORZ ICG Imaging System is a medical device that received FDA 510(k) clearance on 2023-11-06. It is manufactured by Karl Storz SE & CO. KG. The 510(k) number is K232857.

When was KARL STORZ ICG Imaging System approved by the FDA?

KARL STORZ ICG Imaging System received FDA 510(k) clearance on 2023-11-06, under approval number K232857.

What company makes KARL STORZ ICG Imaging System?

KARL STORZ ICG Imaging System is manufactured by Karl Storz SE & CO. KG.

What is the FDA product code for KARL STORZ ICG Imaging System?

The FDA product code for KARL STORZ ICG Imaging System is OWN.

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Official Source

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