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 IDK823497
510k NumberK823497
Device Name:WRIGHT CARE
ClassificationStimulator, Nerve, Transcutaneous, For Pain Relief
Applicant DOW CORNING WRIGHT 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeGZJ  
CFR Regulation Number882.5890 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-11-23
Decision Date1983-01-07

Trademark Results [WRIGHT CARE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
WRIGHT CARE
WRIGHT CARE
73596965 1485159 Dead/Cancelled
DOW CORNING CORPORATION
1986-05-05

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