510(k) DEN980003
- Device
- DIAMOND PROBE/PERIO 2000 SYSTEM
- Applicant
- Diamond General Development Corp.
- 510(k) number
- DEN980003
- Product code
- MVH
- Decision
- Unknown (DENG)
- Decision date
- 1998-07-17
- Date received
- 1998-05-18
- Regulation
- 872.1870
- Classification name
- Device, Detection, Sulfide
- Medical specialty
- Dental
- Review panel
- Dental
- Device class
- 2
- Clearance type
- Post-NSE
- Third party reviewed
- N
Related Records
Applicant Contact
- Contact
- DALE E SEAMON
- Address
- 333 Parkland Plz. Ann Arbor MI US 48103 48103
Source Documents
510(k) summary PDF not indicated by FDA