VIEW-LITE, MODEL-SL— 510(k) K802217

Name: FDA 510(k) clearance K802217
Creator: U.S. Food and Drug Administration
Published: 1980-10-23

Substantially Equivalent

Med-Western Electronics, Inc.

FDA 510(k) clearance K802217 for VIEW-LITE, MODEL-SL, Substantially Equivalent on 1980-10-23. Applicant: Med-Western Electronics, Inc.. Device class: 1.

Clearance details

Applicant: Med-Western Electronics, Inc.
Product code: Code IXC
Device class: Class 1
Regulation: 21 CFR 892.1890
Advisory panel: Radiology
Date received: 1980-09-12
Decision date: 1980-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K813100 — BIO-STIMULATOR, MODEL 4001981-11-27
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K802215 — VIEW-LITE, MODEL-S1980-10-23
K802216 — VIEW-LITE, MODEL-DL1980-10-23

Data sourced from openFDA. This site is unofficial and independent of the FDA.