OBS DISPOSABLE ELECTROSURGICAL PADS, MONOPOLAR, BIOPOLAR, MODELS GBS-DM, GBS-DB— 510(k) K102372

Name: FDA 510(k) clearance K102372
Creator: U.S. Food and Drug Administration
Published: 2010-11-03

Substantially Equivalent

Jiangmen City Xinhui Baisheng Medical Equipment CO

FDA 510(k) clearance K102372 for OBS DISPOSABLE ELECTROSURGICAL PADS, MONOPOLAR, BIOPOLAR, MODELS GBS-DM, GBS-DB, Substantially Equivalent on 2010-11-03. Applicant: Jiangmen City Xinhui Baisheng Medical Equipment CO. Device class: 2.

Clearance details

Applicant: Jiangmen City Xinhui Baisheng Medical Equipment CO
Product code: Code GEI
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 2010-08-20
Decision date: 2010-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jiangmen City, Guangdong, CN

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Adverse events under product code GEI

product code GEI

Death: 133
Injury: 7,585
Malfunction: 35,808
Other: 44
Total: 43,570

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.