Clearance Summary
TRACKMASTER received FDA 510(k) clearance under submission number K925839, sponsored by Jas 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 1993-06-24.
- Submission: K925839
- Applicant / Sponsor: Jas Manufacturing Co., Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5380
- Decision date: 1993-06-24
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.