510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K071242Substantially Equivalent

Dbest One Step Occult Blood Test Kits

Ameritek USA, Inc., Everett WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K071242 is the FDA 510(k) clearance record for DBEST ONE STEP OCCULT BLOOD TEST KITS, a class II device, cleared for Ameritek USA, Inc. on under FDA product code KHE (Reagent, Occult Blood). FDA records list 2 510(k) clearances for Ameritek USA, Inc., from to . As of , FDA records show no recalls naming K071242.

Clearance record

Decision date
Received
(308 days to decision)
Product code
KHE Reagent, Occult Blood
Regulation
21 CFR 864.6550
Device class
Class II
Review panel
Hematology
Applicant
Ameritek USA, Inc. 125 130th St. SE, Everett WA
510(k) summary
Statement
Third party review
No

Clearances, product code KHE

Trailing 12 months

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

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