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

CENTRIPREP 100

K Number: K900280 · Decision Feb 16, 1990
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
2
Applicant Total
20
Review Days
29

Basic Information

Device Name
CENTRIPREP 100
K Number
K900280
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2050
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
AMICON, INC.
Date Received
January 18, 1990
Decision Date
February 16, 1990
Product Code
JJP
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
JJP Electrode, Ion Selective (Non-Specified)

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