510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K050352Substantially Equivalent

In-Vitro Diagnostic Vaginitis Test Kit

Ameritek Research, LLC, Mill Creek WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K050352 is the FDA 510(k) clearance record for IN-VITRO DIAGNOSTIC VAGINITIS TEST KIT, a class I device, cleared for Ameritek Research, LLC on under FDA product code JTO (Discs, Strips And Reagents, Microorganism Differentiation). FDA records list one 510(k) clearance for Ameritek Research, LLC. As of , FDA records show no recalls naming K050352.

Clearance record

Decision date
Received
(202 days to decision)
Product code
JTO Discs, Strips And Reagents, Microorganism Differentiation
Regulation
21 CFR 866.2660
Device class
Class I
Review panel
Microbiology
Applicant
Ameritek Research, LLC 15205 3rd Dr. SE, Mill Creek WA
510(k) summary
Statement
Third party review
No

Clearances, product code JTO

Trailing 12 months

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

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