PRE-POWDERED VINYL PATIENT EXAMINATION GLOVE, NON-STERILE— 510(k) K100977
Substantially EquivalentJiangsu Sunshine Plastic Products, Co., Ltd.
FDA 510(k) clearance K100977 for PRE-POWDERED VINYL PATIENT EXAMINATION GLOVE, NON-STERILE, Substantially Equivalent on 2010-08-12. Applicant: Jiangsu Sunshine Plastic Products, Co., Ltd..
Clearance details
- Applicant
- Jiangsu Sunshine Plastic Products, Co., Ltd.
- Product code
- Code LYZ
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Taipei County, TW
Data sourced from openFDA. This site is unofficial and independent of the FDA.