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FDA 510(k)

VIEW-LITE, MODEL-DL

K-Number: K802216 · 1980-10-23

ApplicantMed-Western Electronics, Inc.
Decision Date1980-10-23
Product CodeIXC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIEW-LITE, MODEL-DL is the device name listed in this FDA 510(k) record. The listed applicant is Med-Western Electronics, Inc.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802216. 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 VIEW-LITE, MODEL-DL?

VIEW-LITE, MODEL-DL is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Med-Western Electronics, Inc.. The 510(k) number is K802216.

When did VIEW-LITE, MODEL-DL receive FDA 510(k) clearance?

VIEW-LITE, MODEL-DL received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802216.

Who is the listed applicant for VIEW-LITE, MODEL-DL?

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

What is the FDA product code for VIEW-LITE, MODEL-DL?

The FDA product code for VIEW-LITE, MODEL-DL 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 Med-Western Electronics, 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.

K813100BIO-STIMULATOR, MODEL 400K810225LITRONIC STIMULATORK802217VIEW-LITE, MODEL-SLK802215VIEW-LITE, MODEL-S

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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