SIEMENS QUANTUM 7E11 TRANSRECTAL TRANSDUCER— 510(k) K930052

Name: FDA 510(k) clearance K930052
Creator: U.S. Food and Drug Administration
Published: 1995-01-04

Substantially Equivalent

Siemens Quantum, Inc.

FDA 510(k) clearance K930052 for SIEMENS QUANTUM 7E11 TRANSRECTAL TRANSDUCER, Substantially Equivalent on 1995-01-04. Applicant: Siemens Quantum, Inc.. Device class: 2.

Clearance details

Applicant: Siemens Quantum, Inc.
Product code: Code ITX
Device class: Class 2
Regulation: 21 CFR 892.1570
Advisory panel: Radiology
Date received: 1993-01-06
Decision date: 1995-01-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Issaquah, WA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code ITX

product code ITX

Death: 6
Injury: 137
Malfunction: 2,036
Total: 2,179

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.