Light-Guide Cables
K-Number: K223183 · 2023-01-13
Device Summary
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. The listed applicant is Olympus Winter & Ibe GmbH. The 510(k) number is K223183.
When did Light-Guide Cables receive FDA 510(k) clearance?
Light-Guide Cables received FDA 510(k) clearance on 2023-01-13, under 510(k) number K223183.
Who is the listed applicant for Light-Guide Cables?
The FDA 510(k) record lists Olympus Winter & Ibe GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Light-Guide Cables?
The FDA product code for Light-Guide Cables is HBI.
Other records listing Olympus Winter & Ibe GmbH 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: HBI)
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.