The following data is part of a premarket notification filed by Vision Quest Industries, Inc. with the FDA for Target Sterile Electrode.
| Device ID | K072799 |
| 510k Number | K072799 |
| Device Name: | TARGET STERILE ELECTRODE |
| Classification | Electrode, Cutaneous |
| Applicant | VISION QUEST INDUSTRIES, INC. 18011 MITCHELL SO. Irvine, CA 92614 |
| Contact | Jaime X Pulley |
| Correspondent | Jaime X Pulley VISION QUEST INDUSTRIES, INC. 18011 MITCHELL SO. Irvine, CA 92614 |
| Product Code | GXY |
| CFR Regulation Number | 882.1320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-10-01 |
| Decision Date | 2008-04-24 |
| Summary: | summary |