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FDA 510(k)

XENON LIGHT SOURCE MODEL 5121

K-Number: K952696 · 1995-07-25

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1995-07-25
Product CodeGCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

XENON LIGHT SOURCE MODEL 5121 is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1995-07-25 under 510(k) number K952696. 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 LIGHT SOURCE MODEL 5121?

XENON LIGHT SOURCE MODEL 5121 is a medical device that received FDA 510(k) clearance on 1995-07-25. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K952696.

When did XENON LIGHT SOURCE MODEL 5121 receive FDA 510(k) clearance?

XENON LIGHT SOURCE MODEL 5121 received FDA 510(k) clearance on 1995-07-25, under 510(k) number K952696.

Who is the listed applicant for XENON LIGHT SOURCE MODEL 5121?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for XENON LIGHT SOURCE MODEL 5121?

The FDA product code for XENON LIGHT SOURCE MODEL 5121 is GCT.

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Other records listing Richard Wolf Medical Instruments Corp. as applicant

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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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