OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIM— 510(k) K984066
Substantially EquivalentOmni Intl., Inc.
FDA 510(k) clearance K984066 for OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIM, Substantially Equivalent on 1999-01-13. Applicant: Omni Intl., Inc..
Clearance details
- Applicant
- Omni Intl., Inc.
- Product code
- Code KGO
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Canton, OH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.