The following data is part of a premarket notification filed by Pilling Co. with the FDA for Pilling Hemostatic Clip Applier Forceps.
Device ID | K854916 |
510k Number | K854916 |
Device Name: | PILLING HEMOSTATIC CLIP APPLIER FORCEPS |
Classification | Forceps, General & Plastic Surgery |
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 | GEN |
CFR Regulation Number | 878.4800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-12-09 |
Decision Date | 1986-01-24 |