SPECTRUM DG-P7000 PEDIATRIC CRADLE— 510(k) K933134

Name: FDA 510(k) clearance K933134
Creator: U.S. Food and Drug Administration
Published: 1993-10-07

Substantially Equivalent

Spectrum X-Ray Corp.

FDA 510(k) clearance K933134 for SPECTRUM DG-P7000 PEDIATRIC CRADLE, Substantially Equivalent on 1993-10-07. Applicant: Spectrum X-Ray Corp.. Device class: 1.

Clearance details

Applicant: Spectrum X-Ray Corp.
Product code: Code KXH
Device class: Class 1
Regulation: 21 CFR 892.1830
Advisory panel: Radiology
Date received: 1993-06-28
Decision date: 1993-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westville, NJ, US

Download summary PDF View on FDA.gov ↗

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