510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K183100Substantially Equivalent

Estrogen Receptor Clone 6F11 Ready-to-Use Primary Antibody for Bond, Estrogen Receptor Clone 6F11 Liquid Concentrate Primary Antibody, Novocastra

Leica Biosystems Newcastle Ltd., Newcastle Upon Tyne, GB / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K183100 is the FDA 510(k) clearance record for Estrogen Receptor Clone 6F11 Ready-to-Use Primary Antibody for Bond, Estrogen Receptor Clone 6F11 Liquid Concentrate Primary Antibody, Novocastra, a class II device, cleared for Leica Biosystems Newcastle, Limited on under FDA product code MYA (Immunohistochemistry Antibody Assay, Estrogen Receptor). FDA records list 6 510(k) clearances for Leica Biosystems Newcastle, Limited, from to . As of , FDA records show no recalls naming K183100.

Clearance record

Decision date
Received
(30 days to decision)
Product code
MYA Immunohistochemistry Antibody Assay, Estrogen Receptor
Regulation
21 CFR 864.1860
Device class
Class II
Review panel
Hematology
Applicant
Leica Biosystems Newcastle, Limited Balliol Business Park W., Newcastle Upon Tyne, GB
510(k) summary
Statement
Third party review
No

Clearances, product code MYA

Trailing 12 months

FDA records hold no clearances under product code MYA in the trailing twelve months.

FDA records show no clearances under product code MYA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MYA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260