G.E. XT CEILING TUBE SUSPENSION— 510(k) K902980

Name: FDA 510(k) clearance K902980
Creator: U.S. Food and Drug Administration
Published: 1990-10-23

Substantially Equivalent

Electromek Diagnostic Systems, Inc.

FDA 510(k) clearance K902980 for G.E. XT CEILING TUBE SUSPENSION, Substantially Equivalent on 1990-10-23. Applicant: Electromek Diagnostic Systems, Inc.. Device class: 2.

Clearance details

Applicant: Electromek Diagnostic Systems, Inc.
Product code: Code JAA
Device class: Class 2
Regulation: 21 CFR 892.1650
Advisory panel: Radiology
Date received: 1990-06-26
Decision date: 1990-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Troy, IL, US

Download summary PDF View on FDA.gov ↗

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K902985 — G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN1990-12-19
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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.