The following data is part of a premarket notification filed by Conphar, Inc. with the FDA for Conphar, Wall Aneroid Sphygmomanometer.
| Device ID | K813303 |
| 510k Number | K813303 |
| Device Name: | CONPHAR, WALL ANEROID SPHYGMOMANOMETER |
| 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 | 1981-11-23 |
| Decision Date | 1982-01-22 |