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FDA 510(k)

MULTIPLE IMAGING XENON ARC AUTO LIGH SOURCE

K-Number: K905124 · 1991-01-25

ApplicantRed Wing Imaging, Inc.
Decision Date1991-01-25
Product CodeGCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MULTIPLE IMAGING XENON ARC AUTO LIGH SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Red Wing Imaging, Inc.. It received FDA 510(k) clearance on 1991-01-25 under 510(k) number K905124. 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 MULTIPLE IMAGING XENON ARC AUTO LIGH SOURCE?

MULTIPLE IMAGING XENON ARC AUTO LIGH SOURCE is a medical device that received FDA 510(k) clearance on 1991-01-25. The listed applicant is Red Wing Imaging, Inc.. The 510(k) number is K905124.

When did MULTIPLE IMAGING XENON ARC AUTO LIGH SOURCE receive FDA 510(k) clearance?

MULTIPLE IMAGING XENON ARC AUTO LIGH SOURCE received FDA 510(k) clearance on 1991-01-25, under 510(k) number K905124.

Who is the listed applicant for MULTIPLE IMAGING XENON ARC AUTO LIGH SOURCE?

The FDA 510(k) record lists Red Wing Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIPLE IMAGING XENON ARC AUTO LIGH SOURCE?

The FDA product code for MULTIPLE IMAGING XENON ARC AUTO LIGH SOURCE is GCT.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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