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

ARCHITECT Syphilis TP Reagent, ARCHITECT Syphilis TP Calibrator, ARCHITECT Syphilis TP Control

K Number: K153730 · Decision Jun 15, 2016
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
34
Applicant Total
25
Review Days
170

Basic Information

Device Name
ARCHITECT Syphilis TP Reagent, ARCHITECT Syphilis TP Calibrator, ARCHITECT Syphilis TP Control
K Number
K153730
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3830
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Laboratories
Date Received
December 28, 2015
Decision Date
June 15, 2016
Product Code
LIP
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LIP Enzyme Linked Immunoabsorption Assay, Treponema Pallidum

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