HYCARE LATEX EXAMINATION GLOVE, POWDERED— 510(k) K010875
Substantially EquivalentHycare Intl. Co., Ltd.
FDA 510(k) clearance K010875 for HYCARE LATEX EXAMINATION GLOVE, POWDERED, Substantially Equivalent on 2001-06-07. Applicant: Hycare Intl. Co., Ltd.. Device class: 1.
Clearance details
- Applicant
- Hycare Intl. Co., Ltd.
- Product code
- Code LYY
- Device class
- Class 1
- Regulation
- 21 CFR 880.6250
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Deerfield Beach, FL, US
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More clearances from Hycare Intl. Co., Ltd.
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