The following data is part of a premarket notification filed by Cameron-miller, Inc. with the FDA for Cameron-miller #40-1516.
| Device ID | K822092 |
| 510k Number | K822092 |
| Device Name: | CAMERON-MILLER #40-1516 |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | CAMERON-MILLER, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-07-16 |
| Decision Date | 1982-09-21 |