NEURO PULSE
Stimulator, Nerve, Transcutaneous, For Pain Relief
PARKER LABORATORIES, INC.
The following data is part of a premarket notification filed by Parker Laboratories, Inc. with the FDA for Neuro Pulse.
Pre-market Notification Details
| Device ID | K841400 |
| 510k Number | K841400 |
| Device Name: | NEURO PULSE |
| Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
| Applicant | PARKER LABORATORIES, INC. 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 | 1984-04-03 |
| Decision Date | 1984-06-15 |
Trademark Results [NEURO PULSE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NEURO PULSE 73495138 not registered Dead/Abandoned |
PARKELL PRODUCTS INC. 1984-08-16 |
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