CLIQ DV-300 ASPIRATOR— 510(k) K132308
Substantially EquivalentDing Hwa Co., Ltd.
FDA 510(k) clearance K132308 for CLIQ DV-300 ASPIRATOR, Substantially Equivalent on 2013-12-30. Applicant: Ding Hwa Co., Ltd..
Clearance details
- Applicant
- Ding Hwa Co., Ltd.
- Product code
- Code JCX
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Buffalo, NY, US
Adverse events under product code JCX
product code JCX- Death
- 11
- Malfunction
- 838
- Other
- 1
- Total
- 850
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.