CARESIDE ANALYZER— 510(k) K981610

Substantially Equivalent

Careside, Inc.

FDA 510(k) clearance K981610 for CARESIDE ANALYZER, Substantially Equivalent on 1998-06-25. Applicant: Careside, Inc.. Device class: 1.

Clearance details

Applicant: Careside, Inc.
Product code: Code CEO
Device class: Class 1
Regulation: 21 CFR 862.1580
Advisory panel: Clinical Chemistry
Date received: 1998-04-30
Decision date: 1998-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Culver City, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CEO

K100263 — ELITECH CLINICAL SYSTEMS PHOSPHORUS, URIC ACID MONO SL AND UREA UV SL REAGENTS2011-05-06
K072141 — S40 CLINICAL ANALYZER, S TEST IP, S TEST UA2008-06-24
K041643 — SYNCHRON SYSTEMS PHOSPHORUS (PHS) REAGENT2004-08-18
K030015 — ATAC PAK PHOSPHORUS REAGENT2003-03-07
K022312 — PICCOLO PHOSPHORUS TEST SYSTEM2002-09-05

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.