Clearance Summary
E100A PULSE OXIMETER FINGER SENSOR/PROBE received FDA 510(k) clearance under submission number K954168, sponsored by Epic Medical Equipment Services, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1996-09-12.
- Submission: K954168
- Applicant / Sponsor: Epic Medical Equipment Services, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 1996-09-12
Classification & Regulation
This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.