510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K830870Substantially Equivalent

Polychaco Indirect Hemagglutination

Parasitic Disease Consultants, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830870 is the FDA 510(k) clearance record for POLYCHACO INDIRECT HEMAGGLUTINATION, a class II device, cleared for Parasitic Disease Consultants on under FDA product code GMM (Antigens, Iha, Toxoplasma Gondii). FDA records list 3 510(k) clearances for Parasitic Disease Consultants, from to . As of , FDA records show no recalls naming K830870.

Clearance record

Decision date
Received
(147 days to decision)
Product code
GMM Antigens, Iha, Toxoplasma Gondii
Regulation
21 CFR 866.3780
Device class
Class II
Review panel
Microbiology
Applicant
Parasitic Disease Consultants 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GMM

Trailing 12 months

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

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