DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE— 510(k) K051487
Substantially EquivalentDoctor'S Research Group, Inc.
FDA 510(k) clearance K051487 for DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE, Substantially Equivalent on 2005-12-22. Applicant: Doctor'S Research Group, Inc..
Clearance details
- Applicant
- Doctor'S Research Group, Inc.
- Product code
- Code KHJ
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Plymouth, CT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.