NEY EQUI-HINGE— 510(k) K790290
Substantially EquivalentDeringer-Ney, Inc.
FDA 510(k) clearance K790290 for NEY EQUI-HINGE, Substantially Equivalent on 1979-04-10. Applicant: Deringer-Ney, Inc.. Device class: 1.
Clearance details
- Applicant
- Deringer-Ney, Inc.
- Product code
- Code ECG
- Device class
- Class 1
- Regulation
- 21 CFR 872.6710
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code ECG
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