510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K072393Substantially Equivalent

Elia Dsdna Immunoassay, Model 14-5500-01, Elia Ana Control, Model 83-1004-01

Phadia AB, Portage MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072393 is the FDA 510(k) clearance record for ELIA DSDNA IMMUNOASSAY, MODEL 14-5500-01, ELIA ANA CONTROL, MODEL 83-1004-01, a class II device, cleared for Phadia US, Inc. on under FDA product code LSW (Anti-Dna Antibody, Antigen And Control). FDA records list 56 510(k) clearances for PHADIA AB, from to . As of , FDA records show one recall naming K072393.

Clearance record

Decision date
Received
(102 days to decision)
Product code
LSW Anti-Dna Antibody, Antigen And Control
Regulation
21 CFR 866.5100
Device class
Class II
Review panel
Immunology
Applicant
Phadia US, Inc. 4169 Commercial Ave., Portage MI
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LSW

Trailing 12 months

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

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