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FDA 510(k)

Aptima Combo 2 Assay (Panther System), Aptima Combo 2 Assay (Tigris) System)

K-Number: K200866 · 2020-05-17

ApplicantHologic, Inc.
Decision Date2020-05-17
Product CodeQEP
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

Aptima Combo 2 Assay (Panther System), Aptima Combo 2 Assay (Tigris) System) is a medical device manufactured by Hologic, Inc.. It received FDA 510(k) clearance on 2020-05-17 under approval number K200866. The device is classified under product code QEP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Aptima Combo 2 Assay (Panther System), Aptima Combo 2 Assay (Tigris) System)?

Aptima Combo 2 Assay (Panther System), Aptima Combo 2 Assay (Tigris) System) is a medical device that received FDA 510(k) clearance on 2020-05-17. It is manufactured by Hologic, Inc.. The 510(k) number is K200866.

When was Aptima Combo 2 Assay (Panther System), Aptima Combo 2 Assay (Tigris) System) approved by the FDA?

Aptima Combo 2 Assay (Panther System), Aptima Combo 2 Assay (Tigris) System) received FDA 510(k) clearance on 2020-05-17, under approval number K200866.

What company makes Aptima Combo 2 Assay (Panther System), Aptima Combo 2 Assay (Tigris) System)?

Aptima Combo 2 Assay (Panther System), Aptima Combo 2 Assay (Tigris) System) is manufactured by Hologic, Inc..

What is the FDA product code for Aptima Combo 2 Assay (Panther System), Aptima Combo 2 Assay (Tigris) System)?

The FDA product code for Aptima Combo 2 Assay (Panther System), Aptima Combo 2 Assay (Tigris) System) is QEP.

Related PubMed Literature

PMID: 41966529 Comparison of the AccuPower HIV-1 Quant Kit and Aptima HIV-1 Quant Dx Assay for quantification of HIV-1 plasma viral load. Diagnostic microbiology and infectious disease (2026)

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K191352binx health io CT/NG AssayBinx Health, Inc. K190515Aptima Combo 2 Assay (Panther System)Hologic, Inc. K190441Xpert CT/NG, GeneXpert Dx System, GeneXpert Infinity-48s and GeneXpert Infinity-80 Systems, GeneXpert Infinity-48 System, Xpert Vaginal/Endocervical Specimen Collection, Xpert Urine Specimen Collection Kit, Xpert Swab Specimen Collection KitCepheid K190433cobas TV/MG for use on cobas 6800/8800 systems, cobas TV/MG Positive Control Kit, cobas Buffer Negative Control KitRoche Molecular Systems, Inc. DEN180047Aptima Mycoplasma genitalium AssayHologic, Inc. K200533binx io CT/NG Assay and binx io CT/NG SystemBinx Health, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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