SYNTEX POWDER-FREE NITRILE EXAMINATION GLOVE— 510(k) K020493
Substantially EquivalentSyntex Healthcare Products Co., Ltd.
FDA 510(k) clearance K020493 for SYNTEX POWDER-FREE NITRILE EXAMINATION GLOVE, Substantially Equivalent on 2002-02-26. Applicant: Syntex Healthcare Products Co., Ltd..
Clearance details
- Applicant
- Syntex Healthcare Products Co., Ltd.
- Product code
- Code LZA
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Xinji City, Hebei Province, CN
Adverse events under product code LZA
product code LZA- Other
- 1
- Total
- 1
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.