Coxsackievirus B Blend Monoclonal Antibodies

FDA 510(k) K940471 · Chemicon Intl., Inc.

Substantially Equivalent

510(k) numberK940471

Submission

Device name
Coxsackievirus B Blend Monoclonal Antibodies
Applicant
Chemicon Intl., Inc.
Temecula, CA, US
Received
February 2, 1994
Decision date
September 8, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GNM – Antisera, Fluorescent, Coxsackievirus A 1-24, B 1-6
Device class
Class I (low risk)
Regulation
21 CFR 866.3145
Specialty
Microbiology

Other 510(k)s with product code GNM

510(k)DeviceApplicantDecision
K940472Coxsackievirus B5 Monoclonal AntibodyGNM · Traditional Chemicon Intl., Inc.09/08/1995SE
K936254Cocksackievirus B6 Monoclonal AntibodyGNM · Traditional Light Diagnostics09/08/1995SE
K936253Coxsackievirus B4 Monoclonal AntibodyGNM · Traditional Light Diagnostics09/08/1995SE
K936252Coxsackievirus B@ Monoclonal AntibodyGNM · Traditional Light Diagnostics09/08/1995SE
K936251Coxsackievirus B3 Monoclonal AntibodyGNM · Traditional Light Diagnostics09/08/1995SE
K936145Coxsackievirus B1 Monoclonal AntibodyGNM · Traditional Chemicon Intl., Inc.09/08/1995SE
K936089Coxsackie A24 Virus Monoclonal AntibodyGNM · Traditional Chemicon Intl., Inc.09/08/1995SE
K936073Enterovirus Monocl Antibody Det of Coxsackie A9 VirusGNM · Traditional Chemicon Intl., Inc.09/08/1995SE

More from Chemicon Intl., Inc.

510(k)DeviceDecision
K992252Light Diagnostics Pneumocystis Carinii Dfa, Model 31965LYF · Special 08/10/1999SE
K940473Enterovirus 71 Monoclonal AntibodyGOE · Traditional 09/12/1995SE
K940027Enterovirus Blend Monoclonal AntibodiesGOE · Traditional 09/12/1995SE
K940472Coxsackievirus B5 Monoclonal AntibodyGNM · Traditional 09/08/1995SE
K936145Coxsackievirus B1 Monoclonal AntibodyGNM · Traditional 09/08/1995SE
K936089Coxsackie A24 Virus Monoclonal AntibodyGNM · Traditional 09/08/1995SE
K936073Enterovirus Monocl Antibody Det of Coxsackie A9 VirusGNM · Traditional 09/08/1995SE

Questions and answers

When was Coxsackievirus B Blend Monoclonal Antibodies cleared by the FDA?

Coxsackievirus B Blend Monoclonal Antibodies (K940471) received a 510(k) decision of Substantially Equivalent on September 8, 1995, 583 days after the submission was received.

What is the product code of K940471?

The FDA product code is GNM – Antisera, Fluorescent, Coxsackievirus A 1-24, B 1-6, a Class I (low risk) device regulated under 21 CFR 866.3145.