DYONICS DRILL GUIDE/ISOMETER SYSTEM— 510(k) K880739
Substantially EquivalentDyonics, Inc.
FDA 510(k) clearance K880739 for DYONICS DRILL GUIDE/ISOMETER SYSTEM, Substantially Equivalent on 1988-03-21. Applicant: Dyonics, Inc.. Device class: 1.
Clearance details
- Applicant
- Dyonics, Inc.
- Product code
- Code LXI
- Device class
- Class 1
- Regulation
- 21 CFR 878.4820
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Andover, MA, US
Recent devices under product code LXI
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