KING DIAGNOSTICS CHLORIDE REAGENT— 510(k) K922921

Name: FDA 510(k) clearance K922921
Creator: U.S. Food and Drug Administration
Published: 1992-10-05

Substantially Equivalent

King Diagnostics, Inc.

FDA 510(k) clearance K922921 for KING DIAGNOSTICS CHLORIDE REAGENT, Substantially Equivalent on 1992-10-05. Applicant: King Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: King Diagnostics, Inc.
Product code: Code CHJ
Device class: Class 2
Regulation: 21 CFR 862.1170
Advisory panel: Clinical Chemistry
Date received: 1992-06-17
Decision date: 1992-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CHJ

view all

K010670 — PICCOLO CHLORIDE TEST SYSTEM2001-04-26
K945408 — 340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZER1995-02-22
K943006 — CHLORIDE QVET1994-12-07
K934136 — OLYMPUS CHLORIDE REAGENT, MODIFICATION1993-11-05
K932528 — OLYMPUS CHLORID REAGENT, MODIFIED1993-09-17

More clearances from King Diagnostics, Inc.

view all

K933329 — KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT1993-10-22
K931834 — KING SODIUM/POTASSIUM STANDARD MODIFIED1993-08-25
K931773 — HDL PRECIPITATING REAGENT (DEXTRAN SULFATE)1993-08-16
K931326 — KING DIAGNOSTICS CK REAGENT1993-06-15
K923129 — KING DIAGNOSTICS GLUCOSE (HK) REAGENT1992-11-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.