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FDA 510(k)

cobas Influenza A/B & RSV Nucleic Acid Test for Use on the cobas Liat System

K-Number: K153544 · 2016-07-25

ApplicantIquum, Inc.
Decision Date2016-07-25
Product CodeOCC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

cobas Influenza A/B & RSV Nucleic Acid Test for Use on the cobas Liat System is a medical device manufactured by Iquum, Inc.. It received FDA 510(k) clearance on 2016-07-25 under approval number K153544. The device is classified under product code OCC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the cobas Influenza A/B & RSV Nucleic Acid Test for Use on the cobas Liat System?

cobas Influenza A/B & RSV Nucleic Acid Test for Use on the cobas Liat System is a medical device that received FDA 510(k) clearance on 2016-07-25. It is manufactured by Iquum, Inc.. The 510(k) number is K153544.

When was cobas Influenza A/B & RSV Nucleic Acid Test for Use on the cobas Liat System approved by the FDA?

cobas Influenza A/B & RSV Nucleic Acid Test for Use on the cobas Liat System received FDA 510(k) clearance on 2016-07-25, under approval number K153544.

What company makes cobas Influenza A/B & RSV Nucleic Acid Test for Use on the cobas Liat System?

cobas Influenza A/B & RSV Nucleic Acid Test for Use on the cobas Liat System is manufactured by Iquum, Inc..

What is the FDA product code for cobas Influenza A/B & RSV Nucleic Acid Test for Use on the cobas Liat System?

The FDA product code for cobas Influenza A/B & RSV Nucleic Acid Test for Use on the cobas Liat System is OCC.

Related Clinical Trials

NCT06417853 Influenza A (H7N9) Vaccine Delivered Intradermally by High-density Microarray Patch (HD-MAP) COMPLETED

Related Devices (Code: OCC)

K163266Alere i Influenza A & B, Alere i Influenza A & B Control Swab Kit, Alere i InstrumentAlere Scarborough, Inc. K152579FilmArray Respiratory Panel EZ (RP EZ)Biofire Diagnostics, LLC K161814Solana Influenza A+B AssayQuidel Corporation K161375Alere i RSV, Alere i Instrument, Alere i RSV Control Swab KitAlere Scarborough, Inc. K161220ARIES® Flu A/B & RSV AssayLuminex Corporation K160068FilmArray Respiratory Panel (RP) for use with FilmArray TorchBiofire Diagnostics, LLC

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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