Clearance Summary
GENESIS DM MODEL: 6053000A1 received FDA 510(k) clearance under submission number K101242, sponsored by Honeywell Hommed, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-06-11.
- Submission: K101242
- Applicant / Sponsor: Honeywell Hommed, LLC
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2910
- Decision date: 2010-06-11
Classification & Regulation
This clearance is catalogued under FDA product code DRG and 21 CFR 870.2910, within the Cardiovascular review panel as a Class II device.