510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K961221Substantially Equivalent

Pylori Igg Elisa Test System

Armkel, LLC, Frederick MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K961221 is the FDA 510(k) clearance record for PYLORI IGG ELISA TEST SYSTEM, a class I device, cleared for Armkel, LLC on under FDA product code LYR (Helicobacter Pylori). FDA records list 68 510(k) clearances for Armkel, LLC, from to . As of , FDA records show no recalls naming K961221.

Clearance record

Decision date
Received
(132 days to decision)
Product code
LYR Helicobacter Pylori
Regulation
21 CFR 866.3110
Device class
Class I
Review panel
Microbiology
Applicant
Armkel, LLC 1306f Bailes Ln., Frederick MD
510(k) summary
Summary
Third party review
No

Clearances, product code LYR

Trailing 12 months

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

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