Medical Device
Manufacturing
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K031857Substantially Equivalent

Advia Chemistry Alpha-1 Antitrypsin Assay

Bayer Diagnostics Corp., Tarrytown NY / Traditional, Substantially Equivalent

K031857 is the FDA 510(k) clearance record for ADVIA CHEMISTRY ALPHA-1 ANTITRYPSIN ASSAY, a class II device, cleared for Bayer Diagnostics Corp. on under FDA product code DEM (Alpha-1-Antitrypsin, Antigen, Antiserum, Control). FDA records list 32 510(k) clearances for Bayer Diagnostics Corp., from to . As of , FDA records show no recalls naming K031857.

Clearance record

Decision date
Received
(80 days to decision)
Product code
DEM Alpha-1-Antitrypsin, Antigen, Antiserum, Control
Regulation
21 CFR 866.5130
Device class
Class II
Review panel
Immunology
Applicant
Bayer Diagnostics Corp. 511 Benedict Ave., Tarrytown NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DEM

Trailing 12 months

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

FDA records show no clearances under product code DEM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DEM, 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