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

ABBOTT MULTI-COLLECT SPECIMEN COLLECTION KIT, ABBOTT REAL TIME CT/NG

K Number: K140354 · Decision May 9, 2014
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
44
Applicant Total
17
Review Days
86

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Basic Information

Device Name
ABBOTT MULTI-COLLECT SPECIMEN COLLECTION KIT, ABBOTT REAL TIME CT/NG
K Number
K140354
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3390
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Molecular, Inc.
Date Received
February 12, 2014
Decision Date
May 9, 2014
Product Code
LSL
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
LSL Dna-Reagents, Neisseria

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