CMV CF Antigen

FDA 510(k) K853277 · Hillcrest Biologicals

Substantially Equivalent

510(k) numberK853277

Submission

Device name
CMV CF Antigen
Applicant
Hillcrest Biologicals
Cypress, CA, US
Received
August 5, 1985
Decision date
November 7, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GQI – Antiserum, Cf, Cytomegalovirus
Device class
Class II (moderate risk)
Regulation
21 CFR 866.3175
Specialty
Microbiology

Other 510(k)s with product code GQI

510(k)DeviceApplicantDecision
K952254Enzyme Linked Immunoabsorbent Assay, CytomegalovirusGQI · Traditional Pyramid Biological Corp.11/16/1995SE
K951800CMV Igg Human Serum ControlsGQI · Traditional Pyramid Biological Corp.11/16/1995SE
K942171CMV Early Antigen TestGQI · Traditional Neogenex06/30/1994SE
K883102Virgo (R) Cmv-Igg ElisaGQI · Traditional Electro-Nucleonics, Inc.02/08/1989SE
K875159Detectadot System 2000 CMV Igg TestGQI · Traditional Gull Laboratories, Inc.05/06/1988SE
K863488Enzygnost Anti-Cmv Igg TestGQI · Traditional Behring Diagnostics, Inc.07/20/1987SE
K864420CMV MicroassayGQI · Traditional Diamedix Corp.02/02/1987SE
K861123The Golden Quad Test (CMV)GQI · Traditional Microbiological Research Corp.02/02/1987SE
K862705Cytomegalovirus Igg Eia Test KitGQI · Traditional Labsystems, Inc.10/01/1986SE
K853989Cor Dot CMVGQI · Traditional Cordis Corp.06/13/1986SE

More from Cordis Corp.

510(k)DeviceDecision
K913618Arbovirus Igm Ifa TestGQC · Traditional 12/03/1992SE
K913617Arbovirus Igg Ifa TestGQC · Traditional 12/03/1992SE
K922374Q Fever Igm Ifa TestGPJ · Traditional 10/21/1992SE
K913906Q Fever Igg Ifa TestGPJ · Traditional 10/21/1992SE
K900206Lyme Disease Igm ElisaLSR · Traditional 06/28/1991SE
K896594Ebv Vca Antibody (Igm)LJN · Traditional 01/16/1990SE
K884829Ebv Early Antigen (R+D)JRY · Traditional 04/12/1989SE
K883767Lyme Disease Ifa (Igm)LSR · Traditional 03/15/1989SE
K884591Ebv-Vca Antibody (Igg)GNP · Traditional 01/24/1989SE
K883487Lyme Disease Ifa (Igg)LSR · Traditional 12/13/1988SE

Questions and answers

When was CMV CF Antigen cleared by the FDA?

CMV CF Antigen (K853277) received a 510(k) decision of Substantially Equivalent on November 7, 1985, 94 days after the submission was received.

What is the product code of K853277?

The FDA product code is GQI – Antiserum, Cf, Cytomegalovirus, a Class II (moderate risk) device regulated under 21 CFR 866.3175.