The following data is part of a premarket notification filed by Ethicon, Inc. with the FDA for Ligaclip Titanium Ligating Clip.
| Device ID | K830503 |
| 510k Number | K830503 |
| Device Name: | LIGACLIP TITANIUM LIGATING CLIP |
| Classification | Clip, Implantable |
| Applicant | ETHICON, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FZP |
| CFR Regulation Number | 878.4300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-02-16 |
| Decision Date | 1983-03-08 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 30705036012836 | K830503 | 000 |
| 30705036012829 | K830503 | 000 |
| 30705036012812 | K830503 | 000 |
| 40705036012802 | K830503 | 000 |
| 40705036012796 | K830503 | 000 |
| 40705036012789 | K830503 | 000 |