The following data is part of a premarket notification filed by Aspen Laboratories, Inc. with the FDA for Single Use Blade Electrode.
| Device ID | K780977 |
| 510k Number | K780977 |
| Device Name: | SINGLE USE BLADE ELECTRODE |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | ASPEN LABORATORIES, 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 | 1978-06-09 |
| Decision Date | 1978-06-22 |