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

Simplexa Flu A/B & RSV Direct Gen II, Simplexa Flu A/B & RSV Positive Control Pack

K Number: K201505 · Decision Aug 22, 2020
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
77
Applicant Total
11
Review Days
78

Basic Information

Device Name
Simplexa Flu A/B & RSV Direct Gen II, Simplexa Flu A/B & RSV Positive Control Pack
K Number
K201505
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3980
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DiaSorin Molecular LLC
Date Received
June 5, 2020
Decision Date
August 22, 2020
Product Code
OCC
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
OCC Respiratory Virus Panel Nucleic Acid Assay System

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K202755 Simplexa Congenital CMV Direct and Simplexa Congenital CMV Positive Control Pack
K212147 Simplexa COVID-19 Direct
K192376 Simplexa VZV Swab Direct, Simplexa VZV Positive Control Pack
K190219 Simplexa VZV Direct, Simplexa VZV Positive Control Pack
K183223 Simplexa Bordetella Direct, Simplexa Bordetella Positive Control Pack
K182467 Simplexa GBS Direct, Simplexa GBS Positive Control Pack
K173498 Simplexa Bordetella Direct, Simplexa Bordetella Positive Control Pack
K173798 Simplexa HSV 1 & 2 Direct, Simplexa HSV 1 & 2 Positive Control Pack
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