Bladder Scanner, Model Name:M5— 510(k) K213488

Substantially Equivalent

Suzhou Peaksonic Medical Technology Co., Ltd.

FDA 510(k) clearance K213488 for Bladder Scanner, Model Name:M5, Substantially Equivalent on 2022-07-01. Applicant: Suzhou Peaksonic Medical Technology Co., Ltd..

Clearance details

Applicant: Suzhou Peaksonic Medical Technology Co., Ltd.
Product code: Code IYO
Advisory panel: Radiology
Date received: 2021-11-01
Decision date: 2022-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Suzhou, CN

Download summary PDF View on FDA.gov ↗

Adverse events under product code IYO

product code IYO

Malfunction: 3,339
Total: 3,339

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.