FLEX Monoclonal Rabbit Anti-Human Estrogen Receptor a, Clone EPI, RTU (Dako Onmis)

FDA 510(k) K170028 · Dako Denmark A/S

Substantially Equivalent

510(k) numberK170028

Submission

Device name
FLEX Monoclonal Rabbit Anti-Human Estrogen Receptor a, Clone EPI, RTU (Dako Onmis)
Applicant
Dako Denmark A/S
Golstrup, DK
Received
January 3, 2017
Decision date
December 21, 2017
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 FLEX Monoclonal Rabbit Anti-Human Estrogen Receptor a, Clone EPI, RTU (Dako Onmis) cleared by the FDA?

FLEX Monoclonal Rabbit Anti-Human Estrogen Receptor a, Clone EPI, RTU (Dako Onmis) (K170028) received a 510(k) decision of Substantially Equivalent on December 21, 2017, 352 days after the submission was received.

What is the product code of K170028?

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