Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K061360Substantially Equivalent

Neomarkers Rabbit Monoclonal Anti-Human Estrogen Rece[ptor Antibody (Clone Sp1)

Lab Vision Corp., Fremont CA / Traditional, Substantially Equivalent

K061360 is the FDA 510(k) clearance record for NEOMARKERS RABBIT MONOCLONAL ANTI-HUMAN ESTROGEN RECE[PTOR ANTIBODY (CLONE SP1), a class II device, cleared for Lab Vision Corp. on under FDA product code MYA (Immunohistochemistry Antibody Assay, Estrogen Receptor). FDA records list 2 510(k) clearances for Lab Vision Corp., from to . As of , FDA records show no recalls naming K061360.

Clearance record

Decision date
Received
(42 days to decision)
Product code
MYA Immunohistochemistry Antibody Assay, Estrogen Receptor
Regulation
21 CFR 864.1860
Device class
Class II
Review panel
Hematology
Applicant
Lab Vision Corp. 47777 Warm Springs Blvd., Fremont CA
510(k) summary
Summary PDF
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