510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K830590Substantially Equivalent

Corning 2500 Co-Oximeter

Corning Medical & Scientific, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830590 is the FDA 510(k) clearance record for CORNING 2500 CO-OXIMETER, a class II device, cleared for Corning Medical & Scientific on under FDA product code KHG (Whole Blood Hemoglobin Determination). FDA records list 111 510(k) clearances for Corning Medical & Scientific, from to . As of , FDA records show no recalls naming K830590.

Clearance record

Decision date
Received
(40 days to decision)
Product code
KHG Whole Blood Hemoglobin Determination
Regulation
21 CFR 864.7500
Device class
Class II
Review panel
Hematology
Applicant
Corning Medical & Scientific 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KHG

Trailing 12 months

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

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