Biogenex Monoclonal Anti-Estrogen Receptor(Clone ER88)

FDA 510(k) K013148 · Biogenex Laboratories

Substantially Equivalent

510(k) numberK013148

Submission

Device name
Biogenex Monoclonal Anti-Estrogen Receptor(Clone ER88)
Applicant
Biogenex Laboratories
San Ramon, CA, US
Received
September 20, 2001
Decision date
February 28, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MYA – Immunohistochemistry Antibody Assay, Estrogen Receptor
Device class
Class II (moderate risk)
Regulation
21 CFR 864.1860
Specialty
Hematology

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Questions and answers

When was Biogenex Monoclonal Anti-Estrogen Receptor(Clone ER88) cleared by the FDA?

Biogenex Monoclonal Anti-Estrogen Receptor(Clone ER88) (K013148) received a 510(k) decision of Substantially Equivalent on February 28, 2002, 161 days after the submission was received.

What is the product code of K013148?

The FDA product code is MYA – Immunohistochemistry Antibody Assay, Estrogen Receptor, a Class II (moderate risk) device regulated under 21 CFR 864.1860.