DRG REACTION CHAMBER/SAFETY TIP— 510(k) K012003
Substantially EquivalentDoctor'S Research Group, Inc.
FDA 510(k) clearance K012003 for DRG REACTION CHAMBER/SAFETY TIP, Substantially Equivalent on 2002-02-12. Applicant: Doctor'S Research Group, Inc.. Device class: 2.
Clearance details
- Applicant
- Doctor'S Research Group, Inc.
- Product code
- Code HEI
- Device class
- Class 2
- Regulation
- 21 CFR 884.2660
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wolcott, CT, US
Recent devices under product code HEI
view allMore clearances from Doctor'S Research Group, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.