The following data is part of a premarket notification filed by Kavo America with the FDA for Kavo Corund Handpiece 2013.
| Device ID | K002708 |
| 510k Number | K002708 |
| Device Name: | KAVO CORUND HANDPIECE 2013 |
| Classification | Airbrush |
| Applicant | KAVO AMERICA 340 EAST MAIN ST. Lake Zurich, IL 60047 |
| Contact | John Westermeier |
| Correspondent | John Westermeier KAVO AMERICA 340 EAST MAIN ST. Lake Zurich, IL 60047 |
| Product Code | KOJ |
| CFR Regulation Number | 872.6080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-08-30 |
| Decision Date | 2000-11-28 |