The following data is part of a premarket notification filed by Ethicon Endo-surgery, Llc with the FDA for Endopath Electrosurgery Probe Plus Ii.
| Device ID | K160128 |
| 510k Number | K160128 |
| Device Name: | Endopath Electrosurgery Probe Plus II |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | Ethicon Endo-Surgery, LLC 475 Calle C Guaynabo, PR 00969 |
| Contact | Marjorie Medina |
| Correspondent | David Locke Ethicon Endo-Surgery, LLC 4545 Creek Road Cincinnati, OH 45242 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-01-20 |
| Decision Date | 2016-04-28 |
| Summary: | summary |