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

Xpert® SA Nasal Complete

K Number: K243070 · Decision Oct 25, 2024
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
23
Applicant Total
10
Review Days
28

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Xpert® SA Nasal Complete
K Number
K243070
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
866.1640
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cepheid®
Date Received
September 27, 2024
Decision Date
October 25, 2024
Product Code
NQX
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
NQX System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen

Similar 510(k) Clearances

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

View all

Other Clearances by Cepheid®

K Number Device Name
K250995 Xpert Xpress CoV-2/Flu/RSV plus
K250996 Xpert Xpress CoV-2/Flu/RSV plus
K243730 Xpert C. difficile/Epi
K242109 Xpert® Xpress CoV-2 plus (XPRS-COV2-10)
K243625 Xpert MRSA/SA SSTI
K243405 Xpert vanA
K230440 Xpert® Xpress CoV-2 plus
K231481 Xpert Xpress CoV-2/Flu/RSV plus
K223046 Xpert® FII & FV