510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K811725Substantially Equivalent

Tbg Diagnostic Kit

Immuno Assay Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K811725 is the FDA 510(k) clearance record for TBG DIAGNOSTIC KIT, a class I device, cleared for Immuno Assay Corp. on under FDA product code CEF (Electrophoretic, Protein Fractionation). FDA records list 10 510(k) clearances for Immuno Assay Corp., from to . As of , FDA records show no recalls naming K811725.

Clearance record

Decision date
Received
(22 days to decision)
Product code
CEF Electrophoretic, Protein Fractionation
Regulation
21 CFR 862.1630
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Immuno Assay Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CEF

Trailing 12 months

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

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