510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K170728Substantially Equivalent

E. Histolytica Quik Chek

Techlab, Inc., Blacksburg VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K170728 is the FDA 510(k) clearance record for E. HISTOLYTICA QUIK CHEK, a class II device, cleared for Techlab, Inc. on under FDA product code KHW (Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.). FDA records list 36 510(k) clearances for Techlab, Inc., from to . As of , FDA records show no recalls naming K170728.

Clearance record

Decision date
Received
(90 days to decision)
Product code
KHW Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.
Regulation
21 CFR 866.3220
Device class
Class II
Review panel
Microbiology
Applicant
Techlab, Inc. 2001 Kraft Dr., Blacksburg VA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KHW

Trailing 12 months

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

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