Clearance Summary
CAMBRIDGE MODEL XT1000 received FDA 510(k) clearance under submission number K854283, sponsored by Cambridge Medical Instruments, 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 1985-11-13.
- Submission: K854283
- Applicant / Sponsor: Cambridge Medical Instruments, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5380
- Decision date: 1985-11-13
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.