Cpr Plus

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K926333 ↗

FDA Product Code

LIX

Device Class

Class II

Regulation

21 CFR Part 870.5210

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Eva Empty Solution Container W/3 Lead Transfer Set

  Class II

  FDA 510(k) K890094 Active Cleared 24 May 1989

• Lucae's Ear & Nasal Applicators

  Class I

  FDA 510(k) K832667 Active Cleared 29 Sep 1983

• Pvc Empty Solution Container Enteral Pump Set

  Class II

  FDA 510(k) K890093 Active Cleared 24 Jul 1989

• Say

  Class I

  FDA 510(k) K823118 Active Cleared 7 Jan 1983

• Dermizip Skin Closure Device

  Not classified

  FDA 510(k) K844072 Active Cleared 5 Nov 1984

• Phonatory Function Analyzer Ps-77

  Class I

  FDA 510(k) K832678 Active Cleared 7 Mar 1984

See all devices from Kells Medical, Inc. →