Clearance Summary
JACE MODEL H440 HAND CPM DEVICE received FDA 510(k) clearance under submission number K931016, sponsored by Jace Systems, 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 1994-06-22.
- Submission: K931016
- Applicant / Sponsor: Jace Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5410
- Decision date: 1994-06-22
Classification & Regulation
This clearance is catalogued under FDA product code JFA and 21 CFR 890.5410, within the Physical Medicine review panel as a Class I device.