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

LIAISON NES Group A Strep; LIAISON NES Group A Strep Control Swab Kit

K Number: K260333 · Decision Jun 15, 2026
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
13
Applicant Total
14
Review Days
133

Basic Information

Device Name
LIAISON NES Group A Strep; LIAISON NES Group A Strep Control Swab Kit
K Number
K260333
Device Class
FDA class 2
Clearance Type
Dual Track
Regulation Number
866.2680
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diasorin Molecular, LLC
Date Received
February 2, 2026
Decision Date
June 15, 2026
Product Code
PGX
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
PGX Groups A, C And G Beta-Hemolytic Streptococcus Nucleic Acid Amplification System

Similar 510(k) Clearances

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

View all

Other Clearances by Diasorin Molecular, LLC

K Number Device Name
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
K201505 Simplexa Flu A/B & RSV Direct Gen II, Simplexa Flu A/B & RSV Positive Control Pack
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 →