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

Xpert® FII & FV

K Number: K223046 · Decision Feb 15, 2023
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
4
Applicant Total
10
Review Days
139

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Basic Information

Device Name
Xpert® FII & FV
K Number
K223046
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
864.7280
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cepheid®
Date Received
September 29, 2022
Decision Date
February 15, 2023
Product Code
NPR
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NPR Test, Factor Ii G20210a Mutations, Genomic Dna Pcr

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NPR), 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
K243405 Xpert vanA
K243070 Xpert® SA Nasal Complete
K230440 Xpert® Xpress CoV-2 plus
K231481 Xpert Xpress CoV-2/Flu/RSV plus