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)

KARL STORZ Urological Laser Accessories

K-Number: K230535 · 2023-09-08

Decision Date2023-09-08
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KARL STORZ Urological Laser Accessories is a medical device manufactured by Karl Storz SE & CO. KG. It received FDA 510(k) clearance on 2023-09-08 under approval number K230535. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ Urological Laser Accessories?

KARL STORZ Urological Laser Accessories is a medical device that received FDA 510(k) clearance on 2023-09-08. It is manufactured by Karl Storz SE & CO. KG. The 510(k) number is K230535.

When was KARL STORZ Urological Laser Accessories approved by the FDA?

KARL STORZ Urological Laser Accessories received FDA 510(k) clearance on 2023-09-08, under approval number K230535.

What company makes KARL STORZ Urological Laser Accessories?

KARL STORZ Urological Laser Accessories is manufactured by Karl Storz SE & CO. KG.

What is the FDA product code for KARL STORZ Urological Laser Accessories?

The FDA product code for KARL STORZ Urological Laser Accessories is GEX. This falls under the Gastroenterology category.

Other Devices by Karl Storz SE & CO. KG

View all 24 devices →

Related Devices (Code: GEX)

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.