PATIENT EXAMINATION GLOVES (LATEX)— 510(k) K892300
Substantially EquivalentRyoden Intl., Ltd.
FDA 510(k) clearance K892300 for PATIENT EXAMINATION GLOVES (LATEX), Substantially Equivalent on 1990-01-24. Applicant: Ryoden Intl., Ltd..
Clearance details
- Applicant
- Ryoden Intl., Ltd.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hong Kong, HK
Data sourced from openFDA. This site is unofficial and independent of the FDA.