PROTEX LATEX EXAMINATION GLOVE— 510(k) K900790
Substantially EquivalentSeyen Intl., Inc.
FDA 510(k) clearance K900790 for PROTEX LATEX EXAMINATION GLOVE, Substantially Equivalent on 1990-04-05. Applicant: Seyen Intl., Inc.. Device class: 1.
Clearance details
- Applicant
- Seyen Intl., 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
- Monterey Park, CA, US
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More clearances from Seyen Intl., Inc.
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