SYNTEX PRE-POWDERED LATEX EXAMINATION GLOVE— 510(k) K022092
Substantially EquivalentSyntex Healthcare Products Co., Ltd.
FDA 510(k) clearance K022092 for SYNTEX PRE-POWDERED LATEX EXAMINATION GLOVE, Substantially Equivalent on 2002-09-03. Applicant: Syntex Healthcare Products Co., Ltd..
Clearance details
- Applicant
- Syntex Healthcare Products Co., Ltd.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Xinji City, Hebei Province, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.