510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K924758Substantially Equivalent

Dmi Blood Gas Analyzer/cartridge

Diamond Medical, Inc., Roseville MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K924758 is the FDA 510(k) clearance record for DMI BLOOD GAS ANALYZER/CARTRIDGE, a class II device, cleared for Diamond Medical, Inc. on under FDA product code CHL (Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph). FDA records list 6 510(k) clearances for Diamond Medical, Inc., from to . As of , FDA records show one recall naming K924758.

Clearance record

Decision date
Received
(71 days to decision)
Product code
CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph
Regulation
21 CFR 862.1120
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Diamond Medical, Inc. 2658 Patton Rd., Roseville MN
510(k) summary
Statement
Third party review
No

Clearances, product code CHL

Trailing 12 months
1 clearance under product code CHL in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CHL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260