XRT 600 R/F, WRF 0600— 510(k) K992603

Name: FDA 510(k) clearance K992603
Creator: U.S. Food and Drug Administration
Published: 1999-10-25

Substantially Equivalent

Wuestec Medical, Inc.

FDA 510(k) clearance K992603 for XRT 600 R/F, WRF 0600, Substantially Equivalent on 1999-10-25. Applicant: Wuestec Medical, Inc.. Device class: 2.

Clearance details

Applicant: Wuestec Medical, Inc.
Product code: Code JAA
Device class: Class 2
Regulation: 21 CFR 892.1650
Advisory panel: Radiology
Date received: 1999-08-03
Decision date: 1999-10-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mobile, AL, 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.