Clearance Summary
MAXVIEW DIAGNOSTIC WORKSTATION received FDA 510(k) clearance under submission number K984023, sponsored by Dynamic Healthcare Technologies, 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 1998-12-08.
- Submission: K984023
- Applicant / Sponsor: Dynamic Healthcare Technologies, Inc.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 1998-12-08
Classification & Regulation
This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.