The following data is part of a premarket notification filed by Cameron-miller, Inc. with the FDA for Electrosurgical Device, Model 26-2500.
| Device ID | K935490 |
| 510k Number | K935490 |
| Device Name: | ELECTROSURGICAL DEVICE, MODEL 26-2500 |
| 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 | 1993-11-15 |
| Decision Date | 1994-04-01 |