The following data is part of a premarket notification filed by Vision Quest Industries Inc./ Dba Vq Orthocare with the FDA for Avid If2.
| Device ID | K183692 |
| 510k Number | K183692 |
| Device Name: | Avid IF2 |
| Classification | Interferential Current Therapy |
| Applicant | Vision Quest Industries Inc./ Dba VQ OrthoCare 1390 Decision Street, Suite A Vista, CA 92081 |
| Contact | Mohamed Ouerghi |
| Correspondent | Mohamed Ouerghi Vision Quest Industries Inc./ Dba VQ OrthoCare 1390 Decision Street, Suite A Vista, CA 92081 |
| Product Code | LIH |
| CFR Regulation Number | 882.5890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-12-31 |
| Decision Date | 2019-06-12 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00817717021811 | K183692 | 000 |