Clearance Summary
ESCORT 300 SERIES received FDA 510(k) clearance under submission number K911665, sponsored by Medical Data Electronics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1991-08-29.
- Submission: K911665
- Applicant / Sponsor: Medical Data Electronics
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5300
- Decision date: 1991-08-29
Classification & Regulation
This clearance is catalogued under FDA product code LDD and 21 CFR 870.5300, within the Cardiovascular review panel as a Class II device.