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FDA 510(k)

XENON LIGHT SOURCE

K-Number: K940963 · 1994-04-08

ApplicantIncredivision, Inc.
Decision Date1994-04-08
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

XENON LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Incredivision, Inc.. It received FDA 510(k) clearance on 1994-04-08 under 510(k) number K940963. The device is classified under product code FFS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XENON LIGHT SOURCE?

XENON LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1994-04-08. The listed applicant is Incredivision, Inc.. The 510(k) number is K940963.

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

XENON LIGHT SOURCE received FDA 510(k) clearance on 1994-04-08, under 510(k) number K940963.

Who is the listed applicant for XENON LIGHT SOURCE?

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

What is the FDA product code for XENON LIGHT SOURCE?

The FDA product code for XENON LIGHT SOURCE is FFS.

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 Incredivision, 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.

K940962LIQUID LIGHT 500

Related Devices (Code: FFS)

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.

K072521COOK FIBER OPTIC BUNDLE AND FLEXOR DEFLECTING ACCESS SHEATHCook Urological, Inc.K061622PS SERIESPhotonic Optische Gerate Gesmbh & CokgK063309TRU-CABLETruphatek International, Ltd.K061025ACCUTECH ENDOLITE PROBEAccutech Medical Technologies, Inc.K023633SOVIS OPTIQUE'S ENDOSCOPIC CABLESovis OptiqueK001698MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159Cogent Light Technologies, Inc.

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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