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

Alinity m STI Assay

K Number: K202977 · Decision Apr 29, 2022
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
22
Applicant Total
17
Review Days
576

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Basic Information

Device Name
Alinity m STI Assay
K Number
K202977
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3393
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Molecular, Inc.
Date Received
September 30, 2020
Decision Date
April 29, 2022
Product Code
QEP
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
QEP Nucleic Acid Detection System For Non-Viral Microorganism(S) Causing Sexually Transmitted Infections

Similar 510(k) Clearances

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

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Other Clearances by Abbott Molecular, Inc.

K Number Device Name
K252102 Alinity m HCV
K243489 Alinity m EBV (09N43-095)
K243485 Alinity m CMV
K241921 Alinity m BKV
K241573 Alinity m Resp-4-Plex
K233349 Alinity m HSV 1 & 2 / VZV
K222379 Alinity m STI Assay
K212778 Alinity m EBV AMP Kit (List No. 09N43-095), Alinity m EBV CTRL Kit (List No. 09N43-085), Alinity m EBV CAL Kit (List No. 09N43-075)
K140354 ABBOTT MULTI-COLLECT SPECIMEN COLLECTION KIT, ABBOTT REAL TIME CT/NG
K131508 VYSIS D7S486/CEP 7 FISH PROBE KIT
Search all 17 clearances from Abbott Molecular, Inc. →