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.. Device class: 2.
Clearance details
- Applicant
- Doctor'S Research Group, Inc.
- Product code
- Code KHJ
- Device class
- Class 2
- Regulation
- 21 CFR 874.3620
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Plymouth, CT, US
Recent devices under product code KHJ
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