Light-Guide Cables
K-Number: K223183 · 2023-01-13
ApplicantOlympus Winter & Ibe GmbH
Decision Date2023-01-13
Product CodeHBI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Light-Guide Cables is a medical device manufactured by Olympus Winter & Ibe GmbH. It received FDA 510(k) clearance on 2023-01-13 under approval number K223183. The device is classified under product code HBI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Light-Guide Cables?
Light-Guide Cables is a medical device that received FDA 510(k) clearance on 2023-01-13. It is manufactured by Olympus Winter & Ibe GmbH. The 510(k) number is K223183.
When was Light-Guide Cables approved by the FDA?
Light-Guide Cables received FDA 510(k) clearance on 2023-01-13, under approval number K223183.
What company makes Light-Guide Cables?
Light-Guide Cables is manufactured by Olympus Winter & Ibe GmbH.
What is the FDA product code for Light-Guide Cables?
The FDA product code for Light-Guide Cables is HBI.
Related Clinical Trials
Other Devices by Olympus Winter & Ibe GmbH
Related Devices (Code: HBI)
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.