LATEX PATIENT EXAMINATION GLOVES— 510(k) K911081
Substantially EquivalentMedical Device Inspection Co., Inc.
FDA 510(k) clearance K911081 for LATEX PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1991-03-21. Applicant: Medical Device Inspection Co., Inc..
Clearance details
- Applicant
- Medical Device Inspection Co., Inc.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Great Neck, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.