MAXICEPTOR
Stimulator, Muscle, Diagnostic
MED GENERAL
The following data is part of a premarket notification filed by Med General with the FDA for Maxiceptor.
Pre-market Notification Details
| Device ID | K780632 |
| 510k Number | K780632 |
| Device Name: | MAXICEPTOR |
| Classification | Stimulator, Muscle, Diagnostic |
| Applicant | MED GENERAL 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ISB |
| CFR Regulation Number | 890.1850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-04-17 |
| Decision Date | 1978-08-14 |
Trademark Results [MAXICEPTOR]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MAXICEPTOR 73121346 1083337 Dead/Cancelled |
Med General, Inc. 1977-04-04 |
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