Clearance Summary
SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH received FDA 510(k) clearance under submission number K891458, sponsored by Back IN Action, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1989-10-20.
- Submission: K891458
- Applicant / Sponsor: Back IN Action, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5850
- Decision date: 1989-10-20
Classification & Regulation
This clearance is catalogued under FDA product code IPF and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.