Flexi-Site (E203-01)/ Flexi-Fit (E300)

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K964055 ↗

FDA Product Code

DQA

Device Class

Class II

Regulation

21 CFR Part 870.2700

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• SPO2 Wrap Sensor

  Class II

  FDA 510(k) K992211 Active Cleared 22 Dec 1999

• Epic SPO2 Finger Sensor, Model E412-20

  Class II

  FDA 510(k) K002223 Active Cleared 22 Aug 2000

• Stat-Shell Disposable SPO2 Sensor

  Class II

  FDA 510(k) K992092 Active Cleared 22 Dec 1999

• E100A Pulse Oximeter Finger Sensor/Probe

  Class II

  FDA 510(k) K954168 Active Cleared 12 Sep 1996

• Transducers for Ultrasound and Tocodynamometer Fetal Monitoring

  Class II

  FDA 510(k) K992811 Active Cleared 18 Jan 2000

• Oximeter Pre-Amp Cable

  Class II

  FDA 510(k) K965172 Active Cleared 16 Jul 1997

See all devices from Epic Medical Equipment Services, Inc. →