SPECTRUM AUTOMATIC CHEST UNIT MODEL C— 510(k) K791811

Name: FDA 510(k) clearance K791811
Creator: U.S. Food and Drug Administration
Published: 1979-10-26

Substantially Equivalent

Spectrum X-Ray Corp.

FDA 510(k) clearance K791811 for SPECTRUM AUTOMATIC CHEST UNIT MODEL C, Substantially Equivalent on 1979-10-26. Applicant: Spectrum X-Ray Corp.. Device class: 2.

Clearance details

Applicant: Spectrum X-Ray Corp.
Product code: Code KPX
Device class: Class 2
Regulation: 21 CFR 892.1860
Advisory panel: Radiology
Date received: 1979-09-18
Decision date: 1979-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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