Clearance Summary
NEOLOOPS received FDA 510(k) clearance under submission number K810890, sponsored by Medical Marketing Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1981-08-31.
- Submission: K810890
- Applicant / Sponsor: Medical Marketing Systems
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class I
- Regulation citation: 21 CFR 870.4500
- Decision date: 1981-08-31
Classification & Regulation
This clearance is catalogued under FDA product code DWS and 21 CFR 870.4500, within the Cardiovascular review panel as a Class I device.