OKLand Patient Return Electrode Pad— 510(k) K183148
Substantially EquivalentAuckland Medical Polymer(Tianjin) Co., Ltd.
FDA 510(k) clearance K183148 for OKLand Patient Return Electrode Pad, Substantially Equivalent on 2020-02-04. Applicant: Auckland Medical Polymer(Tianjin) Co., Ltd..
Clearance details
- Applicant
- Auckland Medical Polymer(Tianjin) Co., Ltd.
- Product code
- Code GEI
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tianjin, CN
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, through . 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.