REGENT BIOGEL DIAGNOSTIC PROCEDURE GLOVE— 510(k) K971514
Substantially EquivalentLondon International Group, Inc.
FDA 510(k) clearance K971514 for REGENT BIOGEL DIAGNOSTIC PROCEDURE GLOVE, Substantially Equivalent on 1997-10-29. Applicant: London International Group, Inc..
Clearance details
- Applicant
- London International Group, Inc.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dotham, AL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.