The following data is part of a premarket notification filed by Valleylab with the FDA for Valleylab G3000 Electrosurgical Instrument.
| Device ID | K051627 |
| 510k Number | K051627 |
| Device Name: | VALLEYLAB G3000 ELECTROSURGICAL INSTRUMENT |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | VALLEYLAB 5920 LONGBOW DR. Boulder, CO 80301 |
| Contact | Herbert Vinson |
| Correspondent | Herbert Vinson VALLEYLAB 5920 LONGBOW DR. Boulder, CO 80301 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-06-20 |
| Decision Date | 2005-07-22 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20884524001934 | K051627 | 000 |
| 20884524000081 | K051627 | 000 |