KARL STORZ Endoscopic Accessories for Urology
K-Number: K252800 · 2026-06-03
Device Summary
Frequently Asked Questions
What is the KARL STORZ Endoscopic Accessories for Urology?
KARL STORZ Endoscopic Accessories for Urology is a medical device that received FDA 510(k) clearance on 2026-06-03. The listed applicant is Karl Storz SE & CO. KG. The 510(k) number is K252800.
When did KARL STORZ Endoscopic Accessories for Urology receive FDA 510(k) clearance?
KARL STORZ Endoscopic Accessories for Urology received FDA 510(k) clearance on 2026-06-03, under 510(k) number K252800.
Who is the listed applicant for KARL STORZ Endoscopic Accessories for Urology?
The FDA 510(k) record lists Karl Storz SE & CO. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KARL STORZ Endoscopic Accessories for Urology?
The FDA product code for KARL STORZ Endoscopic Accessories for Urology is OCZ.
Other records listing Karl Storz SE & CO. KG as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OCZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.