DRG QUICKMIX— 510(k) K011736
Substantially EquivalentDoctor'S Research Group, Inc.
FDA 510(k) clearance K011736 for DRG QUICKMIX, Substantially Equivalent on 2002-01-30. Applicant: Doctor'S Research Group, Inc..
Clearance details
- Applicant
- Doctor'S Research Group, Inc.
- Product code
- Code GXP
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wolcott, CT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.