The following data is part of a premarket notification filed by Cameron-miller, Inc. with the FDA for Model 26-0375, Electrosurgical Generator.
| Device ID | K931541 |
| 510k Number | K931541 |
| Device Name: | MODEL 26-0375, ELECTROSURGICAL GENERATOR |
| Classification | Electrocautery, Gynecologic (and 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 | HGI |
| CFR Regulation Number | 884.4120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-03-29 |
| Decision Date | 1994-06-01 |