KARL STORZ Holders
K-Number: K240506 · 2024-10-22
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.