The following data is part of a premarket notification filed by Pilling Co. with the FDA for Pilling Laparoscopic Instrumentation.
| Device ID | K934427 |
| 510k Number | K934427 |
| Device Name: | PILLING LAPAROSCOPIC INSTRUMENTATION |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | PILLING CO. 420 DELAWARE DR. Fort Washington, PA 19034 |
| Contact | Richard G Jones |
| Correspondent | Richard G Jones PILLING CO. 420 DELAWARE DR. Fort Washington, PA 19034 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-09-10 |
| Decision Date | 1994-01-10 |