Clearance Summary
LIGHT WEIGHT ALUMINUM WALKER received FDA 510(k) clearance under submission number K821404, sponsored by Manuco Manufacturing Co., 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 1982-05-21.
- Submission: K821404
- Applicant / Sponsor: Manuco Manufacturing Co., Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.3825
- Decision date: 1982-05-21
Classification & Regulation
This clearance is catalogued under FDA product code ITJ and 21 CFR 890.3825, within the Physical Medicine review panel as a Class I device.