The following data is part of a premarket notification filed by Zefon Intl. with the FDA for Duracheck Blood Pressure Cuff, Model Zdc4000 Series.
| Device ID | K080366 |
| 510k Number | K080366 |
| Device Name: | DURACHECK BLOOD PRESSURE CUFF, MODEL ZDC4000 SERIES |
| Classification | Blood Pressure Cuff |
| Applicant | ZEFON INTL. 5350 S.W. FIRST LN. Ocala, FL 34474 |
| Contact | Scott Ryan |
| Correspondent | Scott Ryan ZEFON INTL. 5350 S.W. FIRST LN. Ocala, FL 34474 |
| Product Code | DXQ |
| CFR Regulation Number | 870.1120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-02-12 |
| Decision Date | 2008-06-09 |