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

AUTOREADER 2

K Number: K103532 · Decision Aug 26, 2011
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
44
Applicant Total
5
Review Days
268

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Basic Information

Device Name
AUTOREADER 2
K Number
K103532
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.1640
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Trek Diagnostic Systems
Date Received
December 1, 2010
Decision Date
August 26, 2011
Product Code
LRG
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
LRG Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems

Similar 510(k) Clearances

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Other Clearances by Trek Diagnostic Systems

K Number Device Name
K133038 SENSITITRE YEASTONE SUSCEPTIBILITY PLATES
K112276 VIZION
K111615 SENSITITRE 18-24 HR SUSCEPTIBILITY PLATES
K103456 THE SENSITITRE AIM