PATIENT EXAMINATION GLOVES (LATEX)— 510(k) K891267
Substantially EquivalentGenie Rubber Products Co.
FDA 510(k) clearance K891267 for PATIENT EXAMINATION GLOVES (LATEX), Substantially Equivalent on 1989-04-24. Applicant: Genie Rubber Products Co..
Clearance details
- Applicant
- Genie Rubber Products Co.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Roscoe, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.