THYMATRON
Device, Electroconvulsive Therapy
SOMATICS, INC.
The following data is part of a premarket notification filed by Somatics, Inc. with the FDA for Thymatron.
Pre-market Notification Details
| Device ID | K843923 |
| 510k Number | K843923 |
| Device Name: | THYMATRON |
| Classification | Device, Electroconvulsive Therapy |
| Applicant | SOMATICS, INC. 910 SHERWOOD DR., UNIT 17 Lake Bluff, IL 60044 |
| Contact | Richard Abrams |
| Correspondent | Richard Abrams SOMATICS, INC. 910 SHERWOOD DR., UNIT 17 Lake Bluff, IL 60044 |
| Product Code | GXC |
| CFR Regulation Number | 882.5940 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-10-05 |
| Decision Date | 1984-12-03 |
Trademark Results [THYMATRON]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 THYMATRON 75427220 2228364 Live/Registered |
SOMATICS, INC. 1998-02-02 |
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