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FDA 510(k)

LIGHT GUIDE CABLE

K-Number: K111342 · 2011-11-25

ApplicantSchott North America
Decision Date2011-11-25
Product CodeHBI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIGHT GUIDE CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Schott North America. It received FDA 510(k) clearance on 2011-11-25 under 510(k) number K111342. 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 CABLE?

LIGHT GUIDE CABLE is a medical device that received FDA 510(k) clearance on 2011-11-25. The listed applicant is Schott North America. The 510(k) number is K111342.

When did LIGHT GUIDE CABLE receive FDA 510(k) clearance?

LIGHT GUIDE CABLE received FDA 510(k) clearance on 2011-11-25, under 510(k) number K111342.

Who is the listed applicant for LIGHT GUIDE CABLE?

The FDA 510(k) record lists Schott North America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIGHT GUIDE CABLE?

The FDA product code for LIGHT GUIDE CABLE is HBI.

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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.

K223183Light-Guide CablesOlympus Winter & Ibe GmbHK163185OptiLux LED IlluminatorIsolux, LLCK0529791125 XSB XENON FIBER-OPTIC LIGHT SOURCEIsolux, LLCK021931ENDOSCOPIC FIBEROPTIC CABLEGulf Medical FiberopticsK991208ENDOSCOPIC FIBEROPTIC CABLEIsolux AmericaK983277LIGHTSOURCE OR ILLUMINATOR MODEL I-100Cuda Products Co.

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.

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