The following data is part of a premarket notification filed by Conphar, Inc. with the FDA for Conphar Cast Heels.
| Device ID | K803141 |
| 510k Number | K803141 |
| Device Name: | CONPHAR CAST HEELS |
| Classification | Component, Cast |
| Applicant | CONPHAR, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LGF |
| CFR Regulation Number | 888.5940 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-12-12 |
| Decision Date | 1981-01-09 |