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

CLA 200 CHEMPRO(R) LIPID ANALYZER

K Number: K892238 · Decision Jun 7, 1989
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
229
Applicant Total
206
Review Days
64

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Basic Information

Device Name
CLA 200 CHEMPRO(R) LIPID ANALYZER
K Number
K892238
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1175
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Johnson & Johnson Professionals, Inc.
Date Received
April 4, 1989
Decision Date
June 7, 1989
Product Code
CHH
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
CHH Enzymatic Esterase--Oxidase, Cholesterol

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