AII-PRO 100 PLUS AND ALL-PRO 200— 510(k) K991435

Name: FDA 510(k) clearance K991435
Creator: U.S. Food and Drug Administration
Published: 1999-05-20

Substantially Equivalent

All-Pro Imaging Corp.

FDA 510(k) clearance K991435 for AII-PRO 100 PLUS AND ALL-PRO 200, Substantially Equivalent on 1999-05-20. Applicant: All-Pro Imaging Corp.. Device class: 2.

Clearance details

Applicant: All-Pro Imaging Corp.
Product code: Code IXW
Device class: Class 2
Regulation: 21 CFR 892.1900
Advisory panel: Radiology
Date received: 1999-04-26
Decision date: 1999-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hicksville, NY, US

Download summary PDF View on FDA.gov ↗

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