510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K811562Substantially Equivalent

Toxoplasmosis Test Kit

Immuno-Diagnostic Products, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K811562 is the FDA 510(k) clearance record for TOXOPLASMOSIS TEST KIT, a class II device, cleared for Immuno-Diagnostic Products, Inc. on under FDA product code GLZ (Antigens, If, Toxoplasma Gondii). FDA records list 8 510(k) clearances for Immuno-Diagnostic Products, Inc., from to . As of , FDA records show no recalls naming K811562.

Clearance record

Decision date
Received
(43 days to decision)
Product code
GLZ Antigens, If, Toxoplasma Gondii
Regulation
21 CFR 866.3780
Device class
Class II
Review panel
Microbiology
Applicant
Immuno-Diagnostic Products, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GLZ

Trailing 12 months

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

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