Processor, K750 Computer/Data

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K782052 ↗

FDA Product Code

JQP

Device Class

Class I

Regulation

21 CFR Part 862.2100

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• Quantitope 125-I Gentamicin Ria Kit

  Class II

  FDA 510(k) K780323 Active Cleared 17 Mar 1978

• Kallestad Antisera to Tobramycin

  Class II

  FDA 510(k) K812415 Active Cleared 9 Sep 1981

• Ria Kit, Quantitope Cortisol

  Class II

  FDA 510(k) K781903 Active Cleared 26 Jan 1979

• Mark 500 System

  Not classified

  FDA 510(k) K812416 Active Cleared 8 Apr 1982

• Quantimetric Plus C4 Reagent Kit

  Class II

  FDA 510(k) K855012 Active Cleared 26 Feb 1986

• Quanticoat Neonatal 125 T4 Radioimmuno

  Class II

  FDA 510(k) K812611 Active Cleared 2 Oct 1981

See all devices from Kallestad Laboratories, Inc. →