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FDA 510(k)

XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300

K-Number: K924897 · 1993-07-06

Decision Date1993-07-06
Product CodeGCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Devices, Inc.. It received FDA 510(k) clearance on 1993-07-06 under 510(k) number K924897. 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 XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300?

XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300 is a medical device that received FDA 510(k) clearance on 1993-07-06. The listed applicant is Medical Devices, Inc.. The 510(k) number is K924897.

When did XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300 receive FDA 510(k) clearance?

XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300 received FDA 510(k) clearance on 1993-07-06, under 510(k) number K924897.

Who is the listed applicant for XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300?

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

What is the FDA product code for XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300?

The FDA product code for XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300 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.

Other records listing Medical Devices, 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.

View all 49 devices →

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.

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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