MODEL A300CL CLINICAL REFRACTOMETER— 510(k) K941904
Substantially EquivalentVee Gee Scientific, Inc.
FDA 510(k) clearance K941904 for MODEL A300CL CLINICAL REFRACTOMETER, Substantially Equivalent on 1994-12-13. Applicant: Vee Gee Scientific, Inc..
Clearance details
- Applicant
- Vee Gee Scientific, Inc.
- Product code
- Code JRE
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kirkland, WA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.