BD Veritor System for the Rapid Detection of RSV

FDA 510(k) K133140 · Becton, Dickinson & CO

Substantially Equivalent

510(k) numberK133140

Submission

Device name
BD Veritor System for the Rapid Detection of RSV
Applicant
Becton, Dickinson & CO
San Diego, CA, US
Received
October 17, 2013
Decision date
November 15, 2013
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GQG – Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus
Device class
Class I (low risk)
Regulation
21 CFR 866.3480
Specialty
Microbiology

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K162911Sofia RSV FIA on Sofia 2 analyzerGQG · Traditional Quidel Corporation02/22/2017SE
K132456BD Veritor (TM) System for Rapid Detection of RSVGQG · Traditional Becton, Dickinson and Company11/07/2013SE
K130398Sofia(R) RSV FiaGQG · Traditional Quidel Corp.08/13/2013SE
K121633BD Veritor(Tm) System for the Rapid Detection of RSVGQG · Traditional Becton, Dickinson and Company09/18/2012SE
K101918Quickvue RSV 10GQG · Traditional Quidel Corp.09/24/2010SE
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K091235Ramp RSV AssayGQG · Traditional Response Biomedical Corp.07/24/2009SE
K070747Quick Vue RSV Test, Models 20193, 20199GQG · Traditional Quidel Corp.04/23/2007SE

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Questions and answers

When was BD Veritor System for the Rapid Detection of RSV cleared by the FDA?

BD Veritor System for the Rapid Detection of RSV (K133140) received a 510(k) decision of Substantially Equivalent on November 15, 2013, 29 days after the submission was received.

What is the product code of K133140?

The FDA product code is GQG – Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus, a Class I (low risk) device regulated under 21 CFR 866.3480.