HYDRA VISION UROLOGICAL X-RAY SYSTEM— 510(k) K904145

Name: FDA 510(k) clearance K904145
Creator: U.S. Food and Drug Administration
Published: 1990-12-13

Substantially Equivalent

Mallinckrodt Group, Inc.

FDA 510(k) clearance K904145 for HYDRA VISION UROLOGICAL X-RAY SYSTEM, Substantially Equivalent on 1990-12-13. Applicant: Mallinckrodt Group, Inc.. Device class: 2.

Clearance details

Applicant: Mallinckrodt Group, Inc.
Product code: Code KPR
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 1990-09-07
Decision date: 1990-12-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cincinnati, OH, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KPR

product code KPR

Other: 6
Total: 6

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.