LP-Plus

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K903774 ↗

FDA Product Code

DPS

Device Class

Class II

Regulation

21 CFR Part 870.2340

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Instacine

  Class I

  FDA 510(k) K942558 Active Cleared 30 May 1995

• Fluoroplua Cardiac and/or Instaview

  Class II

  FDA 510(k) K941917 Active Cleared 24 Feb 1995

• Instacine D-2000

  Class II

  FDA 510(k) K983088 Active Cleared 22 Sep 1998

• Clinical Electronic Thermometer

  Class II

  FDA 510(k) K841780 Active Cleared 6 Jul 1984

• LP-3 Electrocardiograph

  Class II

  FDA 510(k) K864614 Active Cleared 16 Jun 1987

• Instaspot

  Class II

  FDA 510(k) K942504 Active Cleared 5 May 1995

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