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FDA 510(k)

LILY DARK VIEWER

K-Number: K954998 · 1996-01-29

ApplicantLily Imaging Solutions Co.
Decision Date1996-01-29
Product CodeIXC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LILY DARK VIEWER is the device name listed in this FDA 510(k) record. The listed applicant is Lily Imaging Solutions Co.. It received FDA 510(k) clearance on 1996-01-29 under 510(k) number K954998. 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 LILY DARK VIEWER?

LILY DARK VIEWER is a medical device that received FDA 510(k) clearance on 1996-01-29. The listed applicant is Lily Imaging Solutions Co.. The 510(k) number is K954998.

When did LILY DARK VIEWER receive FDA 510(k) clearance?

LILY DARK VIEWER received FDA 510(k) clearance on 1996-01-29, under 510(k) number K954998.

Who is the listed applicant for LILY DARK VIEWER?

The FDA 510(k) record lists Lily Imaging Solutions Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LILY DARK VIEWER?

The FDA product code for LILY DARK VIEWER is IXC.

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 Lily Imaging Solutions Co. 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.

K954999LILY MULTICANNULA GUIDE

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.K954199VOXBOXVoxelK952188ADVIEWER 2000Adp , Ltd.

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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