The following data is part of a premarket notification filed by Conphar, Inc. with the FDA for Conphar Wall Model Mercury Sphygmoman..
| Device ID | K801182 |
| 510k Number | K801182 |
| Device Name: | CONPHAR WALL MODEL MERCURY SPHYGMOMAN. |
| Classification | Blood Pressure Cuff |
| Applicant | CONPHAR, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DXQ |
| CFR Regulation Number | 870.1120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-05-16 |
| Decision Date | 1980-06-04 |