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

LIAISON Testosterone xt

K Number: K201908 · Decision Oct 15, 2020
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
87
Applicant Total
22
Review Days
98

Basic Information

Device Name
LIAISON Testosterone xt
K Number
K201908
Device Class
FDA class 1
Clearance Type
Special
Regulation Number
862.1680
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DiaSorin Inc.
Date Received
July 9, 2020
Decision Date
October 15, 2020
Product Code
CDZ
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
CDZ Radioimmunoassay, Testosterones And Dihydrotestosterone

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