PATIENT EXAMINATION GLOVES (LATEX)— 510(k) K892622
Substantially EquivalentLatexon Co., Ltd.
FDA 510(k) clearance K892622 for PATIENT EXAMINATION GLOVES (LATEX), Substantially Equivalent on 1989-09-07. Applicant: Latexon Co., Ltd..
Clearance details
- Applicant
- Latexon Co., Ltd.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Denver, CO, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.