The following data is part of a premarket notification filed by Edward Weck, Inc. with the FDA for Hemoclip Surgical Occluding Clip.
| Device ID | K800079 |
| 510k Number | K800079 |
| Device Name: | HEMOCLIP SURGICAL OCCLUDING CLIP |
| Classification | Clip, Implantable |
| Applicant | EDWARD WECK, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FZP |
| CFR Regulation Number | 878.4300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-01-14 |
| Decision Date | 1980-01-28 |