WRIGHT CARE
Stimulator, Nerve, Transcutaneous, For Pain Relief
DOW CORNING WRIGHT
The following data is part of a premarket notification filed by Dow Corning Wright with the FDA for Wright Care.
Pre-market Notification Details
| Device ID | K823497 |
| 510k Number | K823497 |
| Device Name: | WRIGHT CARE |
| Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
| Applicant | DOW CORNING WRIGHT 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GZJ |
| CFR Regulation Number | 882.5890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-11-23 |
| Decision Date | 1983-01-07 |
Trademark Results [WRIGHT CARE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 WRIGHT CARE 73596965 1485159 Dead/Cancelled |
DOW CORNING CORPORATION 1986-05-05 |
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