POWDER FREE LATEX EXAMINATION GLOVE— 510(k) K960467
Substantially EquivalentBiopro, Inc.
FDA 510(k) clearance K960467 for POWDER FREE LATEX EXAMINATION GLOVE, Substantially Equivalent on 1996-05-24. Applicant: Biopro, Inc.. Device class: 1.
Clearance details
- Applicant
- Biopro, Inc.
- 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
- Chester, NJ, US
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More clearances from Biopro, Inc.
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