The following data is part of a premarket notification filed by Kreativ, Inc. with the FDA for Kreativ Model Kv-1.
| Device ID | K940776 |
| 510k Number | K940776 |
| Device Name: | KREATIV MODEL KV-1 |
| Classification | Airbrush |
| Applicant | KREATIV, INC. 1000 SE 160TH AVE. D23 Vancouver, WA 98684 |
| Contact | Charles W Hutchins |
| Correspondent | Charles W Hutchins KREATIV, INC. 1000 SE 160TH AVE. D23 Vancouver, WA 98684 |
| Product Code | KOJ |
| CFR Regulation Number | 872.6080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-02-22 |
| Decision Date | 1994-12-21 |