Hi bebe plus— 510(k) K160274

Substantially Equivalent

Bistos Co., Ltd.

FDA 510(k) clearance K160274 for Hi bebe plus, Substantially Equivalent on 2016-09-01. Applicant: Bistos Co., Ltd..

Clearance details

Applicant: Bistos Co., Ltd.
Product code: Code HGX
Advisory panel: Obstetrics/Gynecology
Date received: 2016-02-02
Decision date: 2016-09-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seongnam-Si, KR

Download summary PDF View on FDA.gov ↗

Adverse events under product code HGX

product code HGX

Injury: 758
Other: 2
Total: 760

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.