The following data is part of a premarket notification filed by Cameron-miller, Inc. with the FDA for Electrosurgical Devices, 26-0330,26-335,340 & 0345.
| Device ID | K854109 |
| 510k Number | K854109 |
| Device Name: | ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345 |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | CAMERON-MILLER, INC. 3949 SOUTH RACINE Chicago, IL 60609 |
| Contact | John W Martin |
| Correspondent | John W Martin CAMERON-MILLER, INC. 3949 SOUTH RACINE Chicago, IL 60609 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-10-08 |
| Decision Date | 1986-01-24 |