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FDA 510(k)

DAYLITE XENON LIGHT SOURCES

K-Number: K013880 · 2001-12-07

ApplicantDesigns For Vision, Inc.
Decision Date2001-12-07
Product CodeGCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAYLITE XENON LIGHT SOURCES is the device name listed in this FDA 510(k) record. The listed applicant is Designs For Vision, Inc.. It received FDA 510(k) clearance on 2001-12-07 under 510(k) number K013880. 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 DAYLITE XENON LIGHT SOURCES?

DAYLITE XENON LIGHT SOURCES is a medical device that received FDA 510(k) clearance on 2001-12-07. The listed applicant is Designs For Vision, Inc.. The 510(k) number is K013880.

When did DAYLITE XENON LIGHT SOURCES receive FDA 510(k) clearance?

DAYLITE XENON LIGHT SOURCES received FDA 510(k) clearance on 2001-12-07, under 510(k) number K013880.

Who is the listed applicant for DAYLITE XENON LIGHT SOURCES?

The FDA 510(k) record lists Designs For Vision, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAYLITE XENON LIGHT SOURCES?

The FDA product code for DAYLITE XENON LIGHT SOURCES 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.

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Other records listing Designs For Vision, 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.

K051786MELIDE FIBEROPTIC LIGHTK043530DVI CURING LIGHTK032283DESIGNS FOR VISION FIBEROPTIC LIGHTK801058ILLUMINATED SPECULUM

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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