The following data is part of a premarket notification filed by Boyd Industries, Inc. with the FDA for Boyd Delivery Unit.
| Device ID | K020833 |
| 510k Number | K020833 |
| Device Name: | BOYD DELIVERY UNIT |
| Classification | Unit, Operative Dental |
| Applicant | BOYD INDUSTRIES, INC. 12900 44TH ST. NORTH Clearwater, FL 33762 |
| Contact | Bruce Livingston |
| Correspondent | Bruce Livingston BOYD INDUSTRIES, INC. 12900 44TH ST. NORTH Clearwater, FL 33762 |
| Product Code | EIA |
| CFR Regulation Number | 872.6640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-03-14 |
| Decision Date | 2002-08-08 |
| Summary: | summary |