PATIENT EXAMINATION GLOVE (LATEX)— 510(k) K892043
Substantially EquivalentMwe Asia America Industries Sdn
FDA 510(k) clearance K892043 for PATIENT EXAMINATION GLOVE (LATEX), Substantially Equivalent on 1989-08-23. Applicant: Mwe Asia America Industries Sdn.
Clearance details
- Applicant
- Mwe Asia America Industries Sdn
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Selangor, MY
Data sourced from openFDA. This site is unofficial and independent of the FDA.