510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K990873Substantially Equivalent

Dbest Urinary Tract Infection Test Kit for Home-Use

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

K990873 is the FDA 510(k) clearance record for DBEST URINARY TRACT INFECTION TEST KIT FOR HOME-USE, a class I device, cleared for Ameritek, Inc. on under FDA product code JMT (Diazo (Colorimetric), Nitrite (Urinary, Non-Quant)). FDA records list 17 510(k) clearances for Ameritek, Inc., from to . As of , FDA records show no recalls naming K990873.

Clearance record

Decision date
Received
(169 days to decision)
Product code
JMT Diazo (Colorimetric), Nitrite (Urinary, Non-Quant)
Regulation
21 CFR 862.1510
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Ameritek, Inc. 7030 35th Ave., NE, Seattle WA
510(k) summary
Statement
Third party review
No

Clearances, product code JMT

Trailing 12 months
1 clearance under product code JMT in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JMT, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260