CARESIDE ANALYZER— 510(k) K993634

Substantially Equivalent

Careside, Inc.

FDA 510(k) clearance K993634 for CARESIDE ANALYZER, Substantially Equivalent on 1999-12-02. Applicant: Careside, Inc.. Device class: 1.

Clearance details

Applicant: Careside, Inc.
Product code: Code JJF
Device class: Class 1
Regulation: 21 CFR 862.2170
Advisory panel: Clinical Chemistry
Date received: 1999-10-27
Decision date: 1999-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Culver City, CA, US

Download summary PDF View on FDA.gov ↗

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K033734 — LIGHTCYCLER INSTRUMENT VERSION 1.22003-12-17
K013654 — PRECISION SYSTEMS ANALETTE CHEMISTRY ANALYZER2002-06-05
K012966 — ROCHE COBAS TAQMAN ANALYZER2002-02-01

More clearances from Careside, Inc.

K020484 — CARESIDE LDH2002-07-03
K020486 — CARESIDE GGT2002-07-01
K020487 — CARESIDE ALT2002-06-04
K020488 — CARESIDE TRGLYCERIDE2002-04-15
K002792 — CARESIDE CHOLINESTERASE2000-11-08

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