510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K984567Substantially Equivalent

Ventana Er Primary Antibody (Clone 6F11)

Ventana, Inc., Tucson AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K984567 is the FDA 510(k) clearance record for VENTANA ER PRIMARY ANTIBODY (CLONE 6F11), a class II device, cleared for Ventana, Inc. on under FDA product code MYA (Immunohistochemistry Antibody Assay, Estrogen Receptor). FDA records list one 510(k) clearance for Ventana, Inc. As of , FDA records show 2 recalls naming K984567.

Clearance record

Decision date
Received
(232 days to decision)
Product code
MYA Immunohistochemistry Antibody Assay, Estrogen Receptor
Regulation
21 CFR 864.1860
Device class
Class II
Review panel
Hematology
Applicant
Ventana, Inc. 3865 N. Business Center, Tucson AZ
510(k) summary
Summary
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