FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CARESIDE CHOLINESTERASE

K Number: K002792 · Decision Nov 8, 2000
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
25
Applicant Total
22
Review Days
62

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Basic Information

Device Name
CARESIDE CHOLINESTERASE
K Number
K002792
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.3240
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Careside, Inc.
Date Received
September 7, 2000
Decision Date
November 8, 2000
Product Code
DIH
Advisory Committee
Clinical Toxicology
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
DIH Colorimetry, Cholinesterase

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DIH), 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
K001462 CARESIDE HEMOGLOBIN
K993771 CARESIDE DIRECT BILIRUBIN
K993634 CARESIDE ANALYZER
K992475 CARESIDE CO2, TOTAL
K991717 CARESIDE MG
K991371 CARESIDE AMMONIA
Search all 22 clearances from Careside, Inc. →