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
32
Registration Numbers
32
Same Product Code
78
Applicant Total
14
Review Days
78

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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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OCC), ordered by most recent decision date.

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Other Clearances by Diasorin Molecular, LLC

K Number Device Name
K260333 LIAISON NES Group A Strep; LIAISON NES Group A Strep Control Swab Kit
K251978 LIAISON NES FLU A/B, RSV & COVID-19
K252387 Simplexa™ COVID-19/ Flu A/B & RSV Direct (MOL4450); Simplexa™ COVID-19/ Flu A/B & RSV Positive Control Pack (MOL4460)
DEN230092 Simplexa C. auris Direct, Simplexa C. auris Positive Control Pack, Simplexa C. auris Sample Prep Kit (MOL3950, MOL3960, MOL5390)
K220963 Simplexa COVID-19 & Flu A/B Direct
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
Search all 14 clearances from Diasorin Molecular, LLC →