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

ABBOTT ARCHITECT TESTOSTERONE

K Number: K983212 · Decision Nov 18, 1998
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
87
Applicant Total
857
Review Days
65

Basic Information

Device Name
ABBOTT ARCHITECT TESTOSTERONE
K Number
K983212
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1680
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ABBOTT LABORATORIES
Date Received
September 14, 1998
Decision Date
November 18, 1998
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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