The following data is part of a premarket notification filed by Neomed Corp. with the FDA for Electrode, Dispersive, Disp. Neopad.
| Device ID | K780118 |
| 510k Number | K780118 |
| Device Name: | ELECTRODE, DISPERSIVE, DISP. NEOPAD |
| Classification | Apparatus, Electrosurgical |
| Applicant | NEOMED CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HAM |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-01-23 |
| Decision Date | 1978-02-23 |