RAYMAX 2100 MODELS 2130 & 2136— 510(k) K883431

Name: FDA 510(k) clearance K883431
Creator: U.S. Food and Drug Administration
Published: 1988-09-12

Substantially Equivalent

Raymax Medical Corp.

FDA 510(k) clearance K883431 for RAYMAX 2100 MODELS 2130 & 2136, Substantially Equivalent on 1988-09-12. Applicant: Raymax Medical Corp.. Device class: 1.

Clearance details

Applicant: Raymax Medical Corp.
Product code: Code IZO
Device class: Class 1
Regulation: 21 CFR 892.1700
Advisory panel: Radiology
Date received: 1988-08-15
Decision date: 1988-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ontario, L4l 7k5, CA

Download summary PDF View on FDA.gov ↗

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