LATEX PATIENT EXAMINATION GLOVE— 510(k) K960942
Substantially EquivalentSiam Sempermed Corp., Ltd.
FDA 510(k) clearance K960942 for LATEX PATIENT EXAMINATION GLOVE, Substantially Equivalent on 1996-09-17. Applicant: Siam Sempermed Corp., Ltd.. Device class: 1.
Clearance details
- Applicant
- Siam Sempermed Corp., 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
- Clearwater, FL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.