AXIOM STABLE II URIC ACID TEST— 510(k) K842442

Substantially Equivalent

Axiom, Inc.

FDA 510(k) clearance K842442 for AXIOM STABLE II URIC ACID TEST, Substantially Equivalent on 1984-08-16. Applicant: Axiom, Inc.. Device class: 1.

Clearance details

Applicant: Axiom, Inc.
Product code: Code KNK
Device class: Class 1
Regulation: 21 CFR 862.1775
Advisory panel: Clinical Chemistry
Date received: 1984-06-21
Decision date: 1984-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Axiom, Inc.

K883887 — AXIOM ATRAUM WOUND DRAINS1989-02-17
K842443 — AXIOM STABLE II TRIGLYCERIDES TEST1984-09-13
K842441 — AXIOM STABLE II CHOLESTEROL TEST1984-07-25

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