ANTELOPE BRAND PATIENT EXAMINATION GLOVES— 510(k) K892781
Substantially EquivalentLiaoning-Usa Corp.
FDA 510(k) clearance K892781 for ANTELOPE BRAND PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1989-09-21. Applicant: Liaoning-Usa Corp..
Clearance details
- Applicant
- Liaoning-Usa Corp.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Pasadena, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.