Treadmill E-17

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K850044 ↗

FDA Product Code

IOL

Device Class

Class I

Regulation

21 CFR Part 890.5380

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Cardioguard Stress Test Monitor 4002

  Class II

  FDA 510(k) K850043 Active Cleared 8 Feb 1985

• Holter PacerCorder

  Class II

  FDA 510(k) K950020 Active Cleared 17 Aug 1995

• Model 9300 Electrocardiovalidator

  Class I

  FDA 510(k) K801830 Active Cleared 27 Aug 1980

• Model 463 Electrocardiorecorder Recorder

  Class II

  FDA 510(k) K884330 Active Cleared 5 Jan 1989

• Holter Digicorder with Pacer Option (Model 483)

  Class II

  FDA 510(k) K963174 Active Cleared 13 Mar 1997

• Ote Biomedical #1296 - 16 Chan. Record

  Class II

  FDA 510(k) K820779 Active Cleared 26 Apr 1982

See all devices from Del Mar Avionics →