KARL STORZ Holders
K-Number: K240506 · 2024-10-22
ApplicantKarl Storz Endoscopy America, Inc.
Decision Date2024-10-22
Product CodeOCV
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
KARL STORZ Holders is a medical device manufactured by Karl Storz Endoscopy America, Inc.. It received FDA 510(k) clearance on 2024-10-22 under approval 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. It is manufactured by Karl Storz Endoscopy America, Inc.. The 510(k) number is K240506.
When was KARL STORZ Holders approved by the FDA?
KARL STORZ Holders received FDA 510(k) clearance on 2024-10-22, under approval number K240506.
What company makes KARL STORZ Holders?
KARL STORZ Holders is manufactured by Karl Storz Endoscopy America, Inc..
What is the FDA product code for KARL STORZ Holders?
The FDA product code for KARL STORZ Holders is OCV.
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K162992Karl Storz UROMAT E.A.S.I.
K162880TIPCAM 1S 3D System
K162410TIPCAM 1S 3D System
Related Devices (Code: OCV)
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.