White Sun Light Source Model #: XL300 and #: XL175

FDA 510(k) K963227 · Products For Medicine

Substantially Equivalent

510(k) numberK963227

Submission

Device name
White Sun Light Source Model #: XL300 and #: XL175
Applicant
Products For Medicine
La Quinta, CA, US
Received
August 19, 1996
Decision date
October 23, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
GCT – Light Source, Endoscope, Xenon Arc
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

Other 510(k)s with product code GCT

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K070376Conmed Linvatec 300W Xenon Light SourceGCT · Traditional Conmed Linvatec08/20/2007SE
K040949Viaduct Miniscope and AccessoriesGCT · Traditional Acueity, Inc.05/07/2004SE
K022490Ksea Medi PackGCT · Traditional KARL STORZ Endoscopy-America, Inc.09/29/2003SE
K031994Linvatec 300W Xenon Light SourceGCT · Traditional Linvatec Corp.08/21/2003SE
K023468Endoscopic Light Source XL180/L3GCT · Traditional World of Medicine Lemke GmbH01/14/2003SE
K021717Endoscopic Light Source, Model XL300/L5GCT · Traditional World of Medicine Lemke GmbH08/20/2002SE
K020889Endoscopic Light Source XL202/L3GCT · Traditional World of Medicine Lemke GmbH06/05/2002SE
K013880Daylite Xenon Light SourcesGCT · Traditional Designs For Vision, Inc.12/07/2001SE

More from Designs For Vision, Inc.

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K953089I-SpouseLYU · Traditional 10/16/1995SE
K951704Non-Woven Filter Paper for Steam and Gas SterilizationFRG · Traditional 06/28/1995SE
K951703Tamper Evident Arrows with and Without Sterilization IndicatorsLRT · Traditional 06/28/1995SE
K883658I-Spose Eye ShieldFXX · Traditional 10/25/1988SE

Questions and answers

When was White Sun Light Source Model #: XL300 and #: XL175 cleared by the FDA?

White Sun Light Source Model #: XL300 and #: XL175 (K963227) received a 510(k) decision of Substantially Equivalent on October 23, 1996, 65 days after the submission was received.

What is the product code of K963227?

The FDA product code is GCT – Light Source, Endoscope, Xenon Arc, a Class II (moderate risk) device regulated under 21 CFR 876.1500.