DIAMOND PROBE/PERIO 2000 SYSTEM
FDA 510(k) clearance DEN980003 · decided 1998-07-17
Clearance details
- K-number
- DEN980003
- Device name
- DIAMOND PROBE/PERIO 2000 SYSTEM
- Applicant
- Diamond General Development Corp.
- Decision
- Unknown
- Date received
- 1998-05-18
- Decision date
- 1998-07-17
- Days to decision
- 60 days
- Clearance type
- Post-NSE
- Product code
- MVH
- Device class
- 2
- Regulation number
- 872.1870
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Ann Arbor, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.