Api Mds*

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K823785 ↗

FDA Product Code

JQP

Device Class

Class I

Regulation

21 CFR Part 862.2100

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• Api 50 E

  Class I

  FDA 510(k) K770989 Active Cleared 29 Jun 1977

• Aso Sure Plus

  Class I

  FDA 510(k) K820786 Active Cleared 8 Apr 1982

• Api 20GP

  Class I

  FDA 510(k) K830525 Active Cleared 18 May 1983

• Aladin (TM)

  Class II

  FDA 510(k) K865062 Active Cleared 25 Mar 1987

• Artap Arterial Blood Sampling Device

  Class I

  FDA 510(k) K843360 Active Cleared 31 Oct 1984

• Referee Bft Blood for Tonometry

  Class I

  FDA 510(k) K792447 Active Cleared 27 Dec 1979

See all devices from Analytical Products, Inc. →