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

Xpert vanA

K Number: K243405 · Decision Nov 21, 2024
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
5
Applicant Total
10
Review Days
20

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Basic Information

Device Name
Xpert vanA
K Number
K243405
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
November 1, 2024
Decision Date
November 21, 2024
Product Code
NIJ
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
NIJ System, Test, Genotypic Detection, Resistant Markers, Enterococcus Species

Similar 510(k) Clearances

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

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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
K243070 Xpert® SA Nasal Complete
K230440 Xpert® Xpress CoV-2 plus
K231481 Xpert Xpress CoV-2/Flu/RSV plus
K223046 Xpert® FII & FV