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FDA 510(k)

LUMENON XENON LIGHT SOURCE

K-Number: K992050 · 1999-09-14

ApplicantWalter Lorenz Surgical, Inc.
Decision Date1999-09-14
Product CodeGCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LUMENON XENON LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Walter Lorenz Surgical, Inc.. It received FDA 510(k) clearance on 1999-09-14 under 510(k) number K992050. 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 LUMENON XENON LIGHT SOURCE?

LUMENON XENON LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1999-09-14. The listed applicant is Walter Lorenz Surgical, Inc.. The 510(k) number is K992050.

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

LUMENON XENON LIGHT SOURCE received FDA 510(k) clearance on 1999-09-14, under 510(k) number K992050.

Who is the listed applicant for LUMENON XENON LIGHT SOURCE?

The FDA 510(k) record lists Walter Lorenz Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LUMENON XENON LIGHT SOURCE?

The FDA product code for LUMENON XENON LIGHT SOURCE is GCT.

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Other records listing Walter Lorenz Surgical, Inc. 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.

K063386LORENZ ORTHODONTIC ANCHORAGE SYSTEMK063052LORENZ TITANIUM FRACTURE / RECONSTRUCTION DEVICES AND PRE-BENT PLATESK063506LORENZ STERNAL CLOSURE SYSTEMK062842TWIST DRILLK061384LORENZ PECTUS SUPPORT BAR, TITANIUM; LORENZ PECTUS SUPPORT BAR STABILIZER, TITANIUMK042516OTOMIMIX

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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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