WEINMANNCOMFORT 2, MODEL WM 27600 AND WEINMANNAQUA, MODEL WM 27603— 510(k) K071163
Substantially EquivalentWeinmann Gerate Fur Medizin GmbH + Co. KG
FDA 510(k) clearance K071163 for WEINMANNCOMFORT 2, MODEL WM 27600 AND WEINMANNAQUA, MODEL WM 27603, Substantially Equivalent on 2007-07-18. Applicant: Weinmann Gerate Fur Medizin GmbH + Co. KG.
Clearance details
- Applicant
- Weinmann Gerate Fur Medizin GmbH + Co. KG
- Product code
- Code BZD
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hamburg, DE
Adverse events under product code BZD
product code BZD- Death
- 4,440
- Injury
- 53,099
- Malfunction
- 213,222
- Other
- 17
- Total
- 270,778
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.