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 |