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FDA 510(k)

ULTRALITE X-RAY FILM ILLUMINATOR

K-Number: K922848 · 1992-09-28

ApplicantA & S Trading Co.
Decision Date1992-09-28
Product CodeIXC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ULTRALITE X-RAY FILM ILLUMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is A & S Trading Co.. It received FDA 510(k) clearance on 1992-09-28 under 510(k) number K922848. The device is classified under product code IXC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRALITE X-RAY FILM ILLUMINATOR?

ULTRALITE X-RAY FILM ILLUMINATOR is a medical device that received FDA 510(k) clearance on 1992-09-28. The listed applicant is A & S Trading Co.. The 510(k) number is K922848.

When did ULTRALITE X-RAY FILM ILLUMINATOR receive FDA 510(k) clearance?

ULTRALITE X-RAY FILM ILLUMINATOR received FDA 510(k) clearance on 1992-09-28, under 510(k) number K922848.

Who is the listed applicant for ULTRALITE X-RAY FILM ILLUMINATOR?

The FDA 510(k) record lists A & S Trading Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRALITE X-RAY FILM ILLUMINATOR?

The FDA product code for ULTRALITE X-RAY FILM ILLUMINATOR is IXC.

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Related Devices (Code: IXC)

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.

K991302SMARTLIGHT DIGITAL FILM VIEWER, MODELS SL 4000PLUS, SL 2000PLUSSmartlight, Inc.K973965SMART MOTORIZED VIEWERSmartlight, Ltd.K973115ARRIPRO 35 ST/TVArnold & Richter Cine TechnikK970240DIFFUSER PANELFocused Viewer, Inc.K954998LILY DARK VIEWERLily Imaging Solutions Co.K954199VOXBOXVoxel

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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