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FDA 510(k)

KARL STORZ Holders

K-Number: K240506 · 2024-10-22

Decision Date2024-10-22
Product CodeOCV
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KARL STORZ Holders is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz Endoscopy America, Inc.. It received FDA 510(k) clearance on 2024-10-22 under 510(k) number K240506. The device is classified under product code OCV. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ Holders?

KARL STORZ Holders is a medical device that received FDA 510(k) clearance on 2024-10-22. The listed applicant is Karl Storz Endoscopy America, Inc.. The 510(k) number is K240506.

When did KARL STORZ Holders receive FDA 510(k) clearance?

KARL STORZ Holders received FDA 510(k) clearance on 2024-10-22, under 510(k) number K240506.

Who is the listed applicant for KARL STORZ Holders?

The FDA 510(k) record lists Karl Storz Endoscopy America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KARL STORZ Holders?

The FDA product code for KARL STORZ Holders is OCV.

Other records listing Karl Storz Endoscopy America, Inc. 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.

View all 52 devices →

Related Devices (Code: OCV)

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

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