The following data is part of a premarket notification filed by Conphar, Inc. with the FDA for Backhaus Clamp, 3 1/2.
| Device ID | K821298 |
| 510k Number | K821298 |
| Device Name: | BACKHAUS CLAMP, 3 1/2 |
| Classification | Forceps |
| Applicant | CONPHAR, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HTD |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-05-04 |
| Decision Date | 1982-05-28 |