AZ 92— 510(k) K931974

Substantially Equivalent

A2j, Inc.

FDA 510(k) clearance K931974 for AZ 92, Substantially Equivalent on 1993-10-08. Applicant: A2j, Inc.. Device class: 1.

Clearance details

Applicant: A2j, Inc.
Product code: Code IWE
Device class: Class 1
Regulation: 21 CFR 892.5780
Advisory panel: Radiology
Date received: 1993-04-22
Decision date: 1993-10-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fredericksburg, VA, US

Download summary PDF View on FDA.gov ↗

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