POWDER FREE VINYL PATIENT EXAMINATION GLOVES— 510(k) K102099
Substantially EquivalentHong DI Plastic Products Co., Ltd.
FDA 510(k) clearance K102099 for POWDER FREE VINYL PATIENT EXAMINATION GLOVES, Substantially Equivalent on 2010-10-06. Applicant: Hong DI Plastic Products Co., Ltd.. Device class: 1.
Clearance details
- Applicant
- Hong DI Plastic Products Co., Ltd.
- Product code
- Code LYZ
- Device class
- Class 1
- Regulation
- 21 CFR 880.6250
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chino, CA, US
Recent devices under product code LYZ
view allMore clearances from Hong DI Plastic Products Co., Ltd.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.