HOOK ELECTRODE, NEEDLE ELECTRODE, COAGULATION BUTTON ELECTRODE— 510(k) K973341
Substantially EquivalentRichard Wolf Medical Instruments Corp.
FDA 510(k) clearance K973341 for HOOK ELECTRODE, NEEDLE ELECTRODE, COAGULATION BUTTON ELECTRODE, Substantially Equivalent on 1997-11-13. Applicant: Richard Wolf Medical Instruments Corp.. Device class: 2.
Clearance details
- Applicant
- Richard Wolf Medical Instruments Corp.
- Product code
- Code GEI
- Device class
- Class 2
- Regulation
- 21 CFR 878.4400
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Vernon Hills, IL, US
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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, 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.