FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CARESIDE LYTES, CARESIDE ANALLYZER MODEL 1000

K Number: K990036 · Decision Mar 18, 1999
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
161
Applicant Total
22
Review Days
71

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Basic Information

Device Name
CARESIDE LYTES, CARESIDE ANALLYZER MODEL 1000
K Number
K990036
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1665
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Careside, Inc.
Date Received
January 6, 1999
Decision Date
March 18, 1999
Product Code
JGS
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JGS Electrode, Ion Specific, Sodium

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JGS), ordered by most recent decision date.

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Other Clearances by Careside, Inc.

K Number Device Name
K020484 CARESIDE LDH
K020486 CARESIDE GGT
K020487 CARESIDE ALT
K020488 CARESIDE TRGLYCERIDE
K002792 CARESIDE CHOLINESTERASE
K001462 CARESIDE HEMOGLOBIN
K993771 CARESIDE DIRECT BILIRUBIN
K993634 CARESIDE ANALYZER
K992475 CARESIDE CO2, TOTAL
K991717 CARESIDE MG
Search all 22 clearances from Careside, Inc. →