XISCAN MODEL 1000— 510(k) K852346

Name: FDA 510(k) clearance K852346
Creator: U.S. Food and Drug Administration
Published: 1986-03-10

Substantially Equivalent

Xi Tech

FDA 510(k) clearance K852346 for XISCAN MODEL 1000, Substantially Equivalent on 1986-03-10. Applicant: Xi Tech. Device class: 2.

Clearance details

Applicant: Xi Tech
Product code: Code JAA
Device class: Class 2
Regulation: 21 CFR 892.1650
Advisory panel: Radiology
Date received: 1985-05-31
Decision date: 1986-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Randolph, NJ, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code JAA

product code JAA

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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