Clearance Summary
INSTANT-X, MODELS 1713 & 128 received FDA 510(k) clearance under submission number K042791, sponsored by Ann Arbor Digital Devices. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-07-01.
- Submission: K042791
- Applicant / Sponsor: Ann Arbor Digital Devices
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1680
- Decision date: 2005-07-01
Classification & Regulation
This clearance is catalogued under FDA product code MQB and 21 CFR 892.1680, within the Radiology review panel as a Class II device.