Imagen Respiratory Syncytial Virus Test

FDA 510(k) K854081 · Boots-Celltech Diagnostics, Inc.

Substantially Equivalent

510(k) numberK854081

Submission

Device name
Imagen Respiratory Syncytial Virus Test
Applicant
Boots-Celltech Diagnostics, Inc.
Berkshire, England, GB
Received
October 7, 1985
Decision date
January 3, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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Questions and answers

When was Imagen Respiratory Syncytial Virus Test cleared by the FDA?

Imagen Respiratory Syncytial Virus Test (K854081) received a 510(k) decision of Substantially Equivalent on January 3, 1986, 88 days after the submission was received.

What is the product code of K854081?

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.