The following data is part of a premarket notification filed by Vision Quest Industries, Inc. with the FDA for Surgi Stim.
| Device ID | K982388 |
| 510k Number | K982388 |
| Device Name: | SURGI STIM |
| Classification | Stimulator, Muscle, Powered |
| Applicant | VISION QUEST INDUSTRIES, INC. 1675 SCENIC AVE. Costa Mesa, CA 92626 |
| Contact | Robert R Thauer |
| Correspondent | Robert R Thauer VISION QUEST INDUSTRIES, INC. 1675 SCENIC AVE. Costa Mesa, CA 92626 |
| Product Code | IPF |
| CFR Regulation Number | 890.5850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-07-09 |
| Decision Date | 1998-09-14 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SURGI STIM 78162207 2734944 Dead/Cancelled |
VisionQuest Industries, Inc. 2002-09-09 |
![]() SURGI STIM 75604911 not registered Dead/Abandoned |
VisionQuest Industries, Inc. 1998-12-14 |