ELECTRO-ACUSCOPE
Stimulator, Nerve, Transcutaneous, For Pain Relief
KENNETH J. PURCELL
The following data is part of a premarket notification filed by Kenneth J. Purcell with the FDA for Electro-acuscope.
Pre-market Notification Details
| Device ID | K832442 |
| 510k Number | K832442 |
| Device Name: | ELECTRO-ACUSCOPE |
| Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
| Applicant | KENNETH J. PURCELL 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 | 1983-07-25 |
| Decision Date | 1983-10-31 |
Trademark Results [ELECTRO-ACUSCOPE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ELECTRO-ACUSCOPE 78054631 2517571 Dead/Cancelled |
Biomedical Development Corp. 2001-03-22 |
 ELECTRO-ACUSCOPE 77903761 3828097 Live/Registered |
Biomedical Development Corporation 2009-12-31 |
 ELECTRO-ACUSCOPE 73698495 1498511 Dead/Cancelled |
BIOMEDICAL DEVELOPMENT CORPORATION 1987-11-18 |
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