510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K771444Substantially Equivalent

Qualicheck Tm

The London Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K771444 is the FDA 510(k) clearance record for QUALICHECK TM, a class I device, cleared for The London Co. on under FDA product code JJS (Controls For Blood-Gases, (Assayed And Unassayed)). FDA records list 7 510(k) clearances for The London Co., from to . As of , FDA records show one recall naming K771444.

Clearance record

Decision date
Received
(15 days to decision)
Product code
JJS Controls For Blood-Gases, (Assayed And Unassayed)
Regulation
21 CFR 862.1660
Device class
Class I
Review panel
Clinical Chemistry
Applicant
The London Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JJS

Trailing 12 months

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

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