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FDA 510(k)

XENON LIGHTSOURCE

K-Number: K962365 · 1996-07-18

ApplicantDsp Worldwide
Decision Date1996-07-18
Product CodeGCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

XENON LIGHTSOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Dsp Worldwide. It received FDA 510(k) clearance on 1996-07-18 under 510(k) number K962365. The device is classified under product code GCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XENON LIGHTSOURCE?

XENON LIGHTSOURCE is a medical device that received FDA 510(k) clearance on 1996-07-18. The listed applicant is Dsp Worldwide. The 510(k) number is K962365.

When did XENON LIGHTSOURCE receive FDA 510(k) clearance?

XENON LIGHTSOURCE received FDA 510(k) clearance on 1996-07-18, under 510(k) number K962365.

Who is the listed applicant for XENON LIGHTSOURCE?

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

What is the FDA product code for XENON LIGHTSOURCE?

The FDA product code for XENON LIGHTSOURCE is GCT.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Dsp Worldwide 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.

K962544MICRO DIAMOND-POINT DISSECTION NEEDLESK962371DERMTOME BLADE

Related Devices (Code: GCT)

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.

K093125ALPHAXENON LIGHT 180 W AND 300 WGimmi GmbHK082925XENON-100 SCB LIGHT SOURCE, MODEL 20132620KARL STORZ Endoscopy-America, Inc.K070376CONMED LINVATEC 300W XENON LIGHT SOURCEConmed LinvatecK040949VIADUCT MINISCOPE AND ACCESSORIESAcueity, Inc.K022490KSEA MEDI PACKKARL STORZ Endoscopy-America, Inc.K031994LINVATEC 300W XENON LIGHT SOURCELinvatec Corp.

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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