Clearance Summary
AFFINITY MEDICAL PATIENT CABLE SYSTEM received FDA 510(k) clearance under submission number K980806, sponsored by Affinity Medical Technologies, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1998-03-25.
- Submission: K980806
- Applicant / Sponsor: Affinity Medical Technologies, LLC
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2900
- Decision date: 1998-03-25
Classification & Regulation
This clearance is catalogued under FDA product code DSA and 21 CFR 870.2900, within the Cardiovascular review panel as a Class II device.