Transducer Probe Cover— 510(k) K221278

Name: FDA 510(k) clearance K221278
Creator: U.S. Food and Drug Administration
Published: 2023-01-11

Substantially Equivalent

Hony Medical Co., Ltd.

FDA 510(k) clearance K221278 for Transducer Probe Cover, Substantially Equivalent on 2023-01-11. Applicant: Hony Medical Co., Ltd.. Device class: 2.

Clearance details

Applicant: Hony Medical Co., Ltd.
Product code: Code ITX
Device class: Class 2
Regulation: 21 CFR 892.1570
Advisory panel: Radiology
Date received: 2022-05-03
Decision date: 2023-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taishan, CN

Download summary PDF View on FDA.gov ↗

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More clearances from Hony Medical Co., Ltd.

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K241789 — Non-Sterile Ultrasound Transmission Gels2024-07-24
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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.