510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K111960Substantially Equivalent

Elitech Clinical Systems Carbon Dioxide Electrode, Elitech Clinical Systems Ise Calibrators

ELITechGroup Inc, Bothell WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K111960 is the FDA 510(k) clearance record for ELITECH CLINICAL SYSTEMS CARBON DIOXIDE ELECTRODE, ELITECH CLINICAL SYSTEMS ISE CALIBRATORS, a class II device, cleared for Elitechgroup on under FDA product code KHS (Enzymatic, Carbon-Dioxide). FDA records list 32 510(k) clearances for Elitechgroup, from to . As of , FDA records show no recalls naming K111960.

Clearance record

Decision date
Received
(130 days to decision)
Product code
KHS Enzymatic, Carbon-Dioxide
Regulation
21 CFR 862.1160
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Elitechgroup 21720 23rd Dr. SE Suite 150, Bothell WA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KHS

Trailing 12 months

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

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