PATIENT EXAMINATION GLOVE (LATEX)— 510(k) K891881
Substantially EquivalentCymun Development Sdn Bhd
FDA 510(k) clearance K891881 for PATIENT EXAMINATION GLOVE (LATEX), Substantially Equivalent on 1989-05-25. Applicant: Cymun Development Sdn Bhd.
Clearance details
- Applicant
- Cymun Development Sdn Bhd
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Perak, Malaysia, MY
Data sourced from openFDA. This site is unofficial and independent of the FDA.