The following data is part of a premarket notification filed by Valleylab, Inc. with the FDA for Lectrovac, Valleylab Models.
| Device ID | K791752 |
| 510k Number | K791752 |
| Device Name: | LECTROVAC, VALLEYLAB MODELS |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | VALLEYLAB, 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 | 1979-09-05 |
| Decision Date | 1979-10-04 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10884521039018 | K791752 | 000 |
| 20884521039015 | K791752 | 000 |