The following data is part of a premarket notification filed by Nebrensky Corp. with the FDA for Electro-acuscope-70.
Device ID | K801459 |
510k Number | K801459 |
Device Name: | ELECTRO-ACUSCOPE-70 |
Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
Applicant | NEBRENSKY CORP. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | GZJ |
CFR Regulation Number | 882.5890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1980-06-24 |
Decision Date | 1980-08-20 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ELECTRO-ACUSCOPE-70 73228977 1152251 Dead/Cancelled |
Nebrensky Corporation 1979-08-27 |