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FDA 510(k)

SYSTEM 3000 XENON VIDEOLAP LIGHT

K-Number: K923210 · 1992-10-05

ApplicantCabot Medical Corp.
Decision Date1992-10-05
Product CodeGCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SYSTEM 3000 XENON VIDEOLAP LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Cabot Medical Corp.. It received FDA 510(k) clearance on 1992-10-05 under 510(k) number K923210. 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 SYSTEM 3000 XENON VIDEOLAP LIGHT?

SYSTEM 3000 XENON VIDEOLAP LIGHT is a medical device that received FDA 510(k) clearance on 1992-10-05. The listed applicant is Cabot Medical Corp.. The 510(k) number is K923210.

When did SYSTEM 3000 XENON VIDEOLAP LIGHT receive FDA 510(k) clearance?

SYSTEM 3000 XENON VIDEOLAP LIGHT received FDA 510(k) clearance on 1992-10-05, under 510(k) number K923210.

Who is the listed applicant for SYSTEM 3000 XENON VIDEOLAP LIGHT?

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

What is the FDA product code for SYSTEM 3000 XENON VIDEOLAP LIGHT?

The FDA product code for SYSTEM 3000 XENON VIDEOLAP LIGHT is GCT.

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Other records listing Cabot Medical Corp. 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.

K960148CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENTK946109CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPSK951972CABOT MEDICAL ULTRA FLOW CYSTOURETHROSCOPE SYSTEM WITH OPERATING & DIAGNOSTIC SHEATHSK951714CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBERK941743CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMPK9341153000 ELECTRONIC INSUFFLATOR MODIFICATION

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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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