PATIENT EXAMINATION GLOVES (LATEX)— 510(k) K892047
Substantially EquivalentGainlite Co., Ltd.
FDA 510(k) clearance K892047 for PATIENT EXAMINATION GLOVES (LATEX), Substantially Equivalent on 1989-08-28. Applicant: Gainlite Co., Ltd..
Clearance details
- Applicant
- Gainlite Co., 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.