The following data is part of a premarket notification filed by A & D Engineering, Inc. with the FDA for Modified Model Ua-711 Digital Sphygmonometer.
| Device ID | K871718 |
| 510k Number | K871718 |
| Device Name: | MODIFIED MODEL UA-711 DIGITAL SPHYGMONOMETER |
| Classification | Computer, Blood-pressure |
| Applicant | A & D ENGINEERING, INC. P.O. BOX 32427 San Jose, CA 95152 |
| Contact | Kimio Shibata |
| Correspondent | Kimio Shibata A & D ENGINEERING, INC. P.O. BOX 32427 San Jose, CA 95152 |
| Product Code | DSK |
| CFR Regulation Number | 870.1110 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-05-04 |
| Decision Date | 1987-06-24 |