Clearance Summary
InkSpace Imaging Body Array received FDA 510(k) clearance under submission number K223487, sponsored by Inkspace Imaging, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2022-12-08.
- Submission: K223487
- Applicant / Sponsor: Inkspace Imaging, Inc.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1000
- Decision date: 2022-12-08
Classification & Regulation
This clearance is catalogued under FDA product code MOS and 21 CFR 892.1000, within the Radiology review panel as a Class II device.