AMPRO LATEX EXAM GLOVE— 510(k) K904740
Substantially EquivalentAmerican Pro Latex, Inc.
FDA 510(k) clearance K904740 for AMPRO LATEX EXAM GLOVE, Substantially Equivalent on 1990-10-26. Applicant: American Pro Latex, Inc.. Device class: 1.
Clearance details
- Applicant
- American Pro Latex, 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
- Glenview, IL, US
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More clearances from American Pro Latex, Inc.
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