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FDA 510(k)

LF MOTORIZED RADIOGRAPHIC FILM VIEWER

K-Number: K840607 · 1984-03-05

ApplicantSybron Corp.
Decision Date1984-03-05
Product CodeIXC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LF MOTORIZED RADIOGRAPHIC FILM VIEWER is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1984-03-05 under 510(k) number K840607. 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 LF MOTORIZED RADIOGRAPHIC FILM VIEWER?

LF MOTORIZED RADIOGRAPHIC FILM VIEWER is a medical device that received FDA 510(k) clearance on 1984-03-05. The listed applicant is Sybron Corp.. The 510(k) number is K840607.

When did LF MOTORIZED RADIOGRAPHIC FILM VIEWER receive FDA 510(k) clearance?

LF MOTORIZED RADIOGRAPHIC FILM VIEWER received FDA 510(k) clearance on 1984-03-05, under 510(k) number K840607.

Who is the listed applicant for LF MOTORIZED RADIOGRAPHIC FILM VIEWER?

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

What is the FDA product code for LF MOTORIZED RADIOGRAPHIC FILM VIEWER?

The FDA product code for LF MOTORIZED RADIOGRAPHIC FILM VIEWER is IXC.

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Other records listing Sybron Corp. 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.

K862284SEALITEK854855PROOF ALGINATE IMPRESSION MATERIALK844092DIAGNOSTIC MICROSOPCE SLIDESK842132TYCOS SELF-CHECK/DIGITAL FEVER THERMOK841910KERR SEALAPEX ROOT CANAL SEALERK841732LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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