The following data is part of a premarket notification filed by Emcision, Ltd. with the FDA for Habib Veseal.
| Device ID | K072126 |
| 510k Number | K072126 |
| Device Name: | HABIB VESEAL |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | EMCISION, LTD. LIVER SURGERY, HAMMERSMITH HOSPITAL CAMPUS, DU CANE RD. London, Uk, GB W12 Ohs |
| Contact | Nagy Habib |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2007-08-02 |
| Decision Date | 2007-10-02 |
| Summary: | summary |