ELECTRO-ACUSCOPE-70

Stimulator, Nerve, Transcutaneous, For Pain Relief

NEBRENSKY CORP.

The following data is part of a premarket notification filed by Nebrensky Corp. with the FDA for Electro-acuscope-70.

Pre-market Notification Details

Device IDK801459
510k NumberK801459
Device Name:ELECTRO-ACUSCOPE-70
ClassificationStimulator, Nerve, Transcutaneous, For Pain Relief
Applicant NEBRENSKY CORP. 4221 Richmond Rd., N.W. Walker,  MI  49534
Product CodeGZJ  
CFR Regulation Number882.5890 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1980-06-24
Decision Date1980-08-20

Trademark Results [ELECTRO-ACUSCOPE-70]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ELECTRO-ACUSCOPE-70
ELECTRO-ACUSCOPE-70
73228977 1152251 Dead/Cancelled
Nebrensky Corporation
1979-08-27

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.