LATEX PATIENT EXAMINATION GLOVE (POWDERFREE/HYPOALLERGENIC) (MODIFICATION)— 510(k) K954880
Substantially EquivalentSiam Sempermed Corp., Ltd.
FDA 510(k) clearance K954880 for LATEX PATIENT EXAMINATION GLOVE (POWDERFREE/HYPOALLERGENIC) (MODIFICATION), Substantially Equivalent on 1995-11-15. Applicant: Siam Sempermed Corp., Ltd..
Clearance details
- Applicant
- Siam Sempermed Corp., Ltd.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Clearwater, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.