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

ICON FXHCG URINE/SERUM TEST, ICON FXHCG URINE TEST, MODELS 40025,40050, 40005 & 41025

K Number: K981512 · Decision May 28, 1998
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
374
Applicant Total
1
Review Days
30

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Basic Information

Device Name
ICON FXHCG URINE/SERUM TEST, ICON FXHCG URINE TEST, MODELS 40025,40050, 40005 & 41025
K Number
K981512
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Skd, Inc. A Beckman Coulter Co.
Date Received
April 28, 1998
Decision Date
May 28, 1998
Product Code
JHI
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
JHI Visual, Pregnancy Hcg, Prescription Use

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