510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K831927Substantially Equivalent

Antinuclear Antibody Test Kit

Breit Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K831927 is the FDA 510(k) clearance record for ANTINUCLEAR ANTIBODY TEST KIT, a class II device, cleared for Breit Laboratories, Inc. on under FDA product code DAA (Igg, Peroxidase, Antigen, Antiserum, Control). FDA records list 5 510(k) clearances for Breit Laboratories, Inc., from to . As of , FDA records show no recalls naming K831927.

Clearance record

Decision date
Received
(33 days to decision)
Product code
DAA Igg, Peroxidase, Antigen, Antiserum, Control
Regulation
21 CFR 866.5510
Device class
Class II
Review panel
Immunology
Applicant
Breit Laboratories, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DAA

Trailing 12 months

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

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