Clearance Summary
ORBITER(TM) TREADMILL received FDA 510(k) clearance under submission number K897179, sponsored by Lee-Meredith Industries, 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 1990-02-15.
- Submission: K897179
- Applicant / Sponsor: Lee-Meredith Industries, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5380
- Decision date: 1990-02-15
Classification & Regulation
This clearance is catalogued under FDA product code IOL and 21 CFR 890.5380, within the Physical Medicine review panel as a Class I device.