POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE— 510(k) K070760
Substantially EquivalentDerma Care Plus Products, LLC
FDA 510(k) clearance K070760 for POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE, Substantially Equivalent on 2007-06-07. Applicant: Derma Care Plus Products, LLC. Device class: 1.
Clearance details
- Applicant
- Derma Care Plus Products, LLC
- 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
- Green Bay, WI, US
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More clearances from Derma Care Plus Products, LLC
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