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 |