510(k) K982388
K982388 is an FDA 510(k) premarket notification submitted by Vision Quest Industries, Inc. for the device "SURGI STIM". The FDA issued a decision of Substantially Equivalent on September 14, 1998. The device falls under product code IPF (Stimulator, Muscle, Powered), a Class II device regulated under 21 CFR 890.5850. Vision Quest Industries, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 14, 1998
- Date Received
- July 9, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Muscle, Powered
- Device Class
- Class II
- Regulation Number
- 890.5850
- Review Panel
- PM
- Submission Type