URICACID— 510(k) K821741

Substantially Equivalent

Biodynamics Corp.

FDA 510(k) clearance K821741 for URICACID, Substantially Equivalent on 1982-07-02. Applicant: Biodynamics Corp.. Device class: 1.

Clearance details

Applicant: Biodynamics Corp.
Product code: Code KNK
Device class: Class 1
Regulation: 21 CFR 862.1775
Advisory panel: Clinical Chemistry
Date received: 1982-06-14
Decision date: 1982-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KNK

K102568 — URIC ACID MODEL 3P392011-05-06
K062862 — OLYMPUS URIC ACID REAGENT, MODEL OSR6X982007-04-06
K040467 — VITALAB URIC ACID REAGENT2004-03-08
K031044 — ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATOR2003-07-15
K022096 — URIC ACID ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEM2003-03-18

More clearances from Biodynamics Corp.

K051675 — BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER2006-03-16
K884033 — BIODYNAMICS MODEL 200 BODY COMPOSITION ANALYZER1988-11-17
K881631 — BIODYNAMICS AUTOTRANSFUSION RESERVOIR1988-09-09
K881968 — BIODYNAMICS MODEL BI-400 BODY COMPOSITION ANALYZER1988-07-28
K874361 — BIODYNAMICS MODEL BI-300 BODY COMPOSITION ANALYZER1988-03-16

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