The following data is part of a premarket notification filed by Davis & Geck, Inc. with the FDA for Multiclip Disp. Ligating Clip Device.
| Device ID | K820999 |
| 510k Number | K820999 |
| Device Name: | MULTICLIP DISP. LIGATING CLIP DEVICE |
| Classification | Clip, Implantable |
| Applicant | DAVIS & GECK, 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 | 1982-04-08 |
| Decision Date | 1982-05-13 |