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 |