PATIENT EXAMINATION GLOVES (LATEX)— 510(k) K892109
Substantially EquivalentBrilliant Ray Intl., Inc.
FDA 510(k) clearance K892109 for PATIENT EXAMINATION GLOVES (LATEX), Substantially Equivalent on 1989-05-04. Applicant: Brilliant Ray Intl., Inc..
Clearance details
- Applicant
- Brilliant Ray Intl., Inc.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.