PATIENT EXAMINATION GLOVE (LATEX)— 510(k) K892008
Substantially EquivalentMediglove Sdn. Bhd.
FDA 510(k) clearance K892008 for PATIENT EXAMINATION GLOVE (LATEX), Substantially Equivalent on 1989-04-27. Applicant: Mediglove Sdn. Bhd..
Clearance details
- Applicant
- Mediglove Sdn. Bhd.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hauppauge, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.