The following data is part of a premarket notification filed by Kavo Dental Corporation with the FDA for Diagnodent 2190 With Periodontal Probe.
| Device ID | K060080 |
| 510k Number | K060080 |
| Device Name: | DIAGNODENT 2190 WITH PERIODONTAL PROBE |
| Classification | Caries Detector, Laser Light, Transmission |
| Applicant | KAVO DENTAL CORPORATION PO BOX 7007 Deerfield, IL 60015 |
| Contact | Daniel Kamm |
| Correspondent | Daniel Kamm KAVO DENTAL CORPORATION PO BOX 7007 Deerfield, IL 60015 |
| Product Code | NTK |
| CFR Regulation Number | 872.1745 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-01-10 |
| Decision Date | 2006-02-08 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| EKAV100270000 | K060080 | 000 |