SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWDER FREE— 510(k) K060778
Substantially EquivalentEver Light Plastic Products Co., Ltd.
FDA 510(k) clearance K060778 for SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWDER FREE, Substantially Equivalent on 2006-04-28. Applicant: Ever Light Plastic Products Co., Ltd..
Clearance details
- Applicant
- Ever Light Plastic Products Co., Ltd.
- Product code
- Code LYZ
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chino, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.