DISPOSA-CUF
Blood Pressure Cuff
CREST MEDICAL EQUIPMENT
The following data is part of a premarket notification filed by Crest Medical Equipment with the FDA for Disposa-cuf.
Pre-market Notification Details
| Device ID | K790810 |
| 510k Number | K790810 |
| Device Name: | DISPOSA-CUF |
| Classification | Blood Pressure Cuff |
| Applicant | CREST MEDICAL EQUIPMENT 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | DXQ |
| CFR Regulation Number | 870.1120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-04-26 |
| Decision Date | 1979-05-25 |
Trademark Results [DISPOSA-CUF]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 DISPOSA-CUF 73402991 1266244 Dead/Cancelled |
Johnson & Johnson 1982-11-17 |
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