Clearance Summary
BOGER AUTO-TRACTION DEVICE received FDA 510(k) clearance under submission number K820663, sponsored by D.C. Medical Device, 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 1982-05-03.
- Submission: K820663
- Applicant / Sponsor: D.C. Medical Device, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5925
- Decision date: 1982-05-03
Classification & Regulation
This clearance is catalogued under FDA product code ILZ and 21 CFR 890.5925, within the Physical Medicine review panel as a Class I device.