The following data is part of a premarket notification filed by Pilling Co. with the FDA for Titanium Hemostatic Clips.
| Device ID | K861922 |
| 510k Number | K861922 |
| Device Name: | TITANIUM HEMOSTATIC CLIPS |
| Classification | Clip, Implantable |
| Applicant | PILLING CO. 420 DELAWARE DR. Fort Washington, PA 19034 |
| Contact | Leland J Wimer |
| Correspondent | Leland J Wimer PILLING CO. 420 DELAWARE DR. Fort Washington, PA 19034 |
| Product Code | FZP |
| CFR Regulation Number | 878.4300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-05-19 |
| Decision Date | 1986-06-13 |