The following data is part of a premarket notification filed by Dow Corning Wright with the FDA for Wright Care.
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 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
WRIGHT CARE 73596965 1485159 Dead/Cancelled |
DOW CORNING CORPORATION 1986-05-05 |